ABC transporters probably involved in multidrug resistance. A member of this family confers vinblastine resistance to Leishmania enriettii.
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 17 |
GO:0110165 | cellular anatomical entity | 1 | 17 |
Related structures:
AlphaFold database: A4HFB1
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 17 |
GO:0005215 | transporter activity | 1 | 17 |
GO:0005488 | binding | 1 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0022804 | active transmembrane transporter activity | 3 | 17 |
GO:0022857 | transmembrane transporter activity | 2 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:0140359 | ABC-type transporter activity | 3 | 17 |
GO:0140657 | ATP-dependent activity | 1 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
GO:0003824 | catalytic activity | 1 | 4 |
GO:0016787 | hydrolase activity | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1118 | 1122 | PF00656 | 0.463 |
CLV_C14_Caspase3-7 | 1126 | 1130 | PF00656 | 0.442 |
CLV_C14_Caspase3-7 | 1194 | 1198 | PF00656 | 0.531 |
CLV_C14_Caspase3-7 | 13 | 17 | PF00656 | 0.741 |
CLV_C14_Caspase3-7 | 454 | 458 | PF00656 | 0.441 |
CLV_C14_Caspase3-7 | 486 | 490 | PF00656 | 0.355 |
CLV_C14_Caspase3-7 | 639 | 643 | PF00656 | 0.720 |
CLV_C14_Caspase3-7 | 668 | 672 | PF00656 | 0.658 |
CLV_C14_Caspase3-7 | 993 | 997 | PF00656 | 0.431 |
CLV_NRD_NRD_1 | 1213 | 1215 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.226 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.270 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 683 | 685 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 803 | 805 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 925 | 927 | PF00675 | 0.281 |
CLV_PCSK_FUR_1 | 911 | 915 | PF00082 | 0.155 |
CLV_PCSK_KEX2_1 | 1213 | 1215 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 803 | 805 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 910 | 912 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 913 | 915 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 925 | 927 | PF00082 | 0.243 |
CLV_PCSK_PC1ET2_1 | 910 | 912 | PF00082 | 0.280 |
CLV_PCSK_PC1ET2_1 | 913 | 915 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 1000 | 1004 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 1185 | 1189 | PF00082 | 0.234 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.226 |
CLV_PCSK_SKI1_1 | 561 | 565 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 692 | 696 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 784 | 788 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 851 | 855 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 907 | 911 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 926 | 930 | PF00082 | 0.202 |
DEG_APCC_DBOX_1 | 1101 | 1109 | PF00400 | 0.474 |
DEG_APCC_DBOX_1 | 152 | 160 | PF00400 | 0.514 |
DEG_APCC_DBOX_1 | 925 | 933 | PF00400 | 0.514 |
DEG_MDM2_SWIB_1 | 181 | 189 | PF02201 | 0.253 |
DEG_ODPH_VHL_1 | 79 | 91 | PF01847 | 0.155 |
DOC_CYCLIN_RxL_1 | 1182 | 1193 | PF00134 | 0.446 |
DOC_MAPK_FxFP_2 | 1034 | 1037 | PF00069 | 0.442 |
DOC_MAPK_FxFP_2 | 370 | 373 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 389 | 396 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 435 | 443 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 534 | 540 | PF00069 | 0.601 |
DOC_MAPK_gen_1 | 910 | 918 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 925 | 932 | PF00069 | 0.374 |
DOC_MAPK_MEF2A_6 | 1043 | 1052 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 1102 | 1109 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 700 | 708 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 925 | 932 | PF00069 | 0.432 |
DOC_PP1_RVXF_1 | 1016 | 1022 | PF00149 | 0.518 |
DOC_PP1_RVXF_1 | 364 | 371 | PF00149 | 0.487 |
DOC_PP1_RVXF_1 | 391 | 397 | PF00149 | 0.433 |
DOC_PP1_RVXF_1 | 782 | 789 | PF00149 | 0.496 |
DOC_PP2B_LxvP_1 | 485 | 488 | PF13499 | 0.426 |
DOC_PP4_FxxP_1 | 1034 | 1037 | PF00568 | 0.442 |
DOC_PP4_FxxP_1 | 370 | 373 | PF00568 | 0.489 |
DOC_PP4_FxxP_1 | 414 | 417 | PF00568 | 0.441 |
DOC_PP4_FxxP_1 | 799 | 802 | PF00568 | 0.432 |
DOC_SPAK_OSR1_1 | 1214 | 1218 | PF12202 | 0.570 |
DOC_USP7_MATH_1 | 1010 | 1014 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 1054 | 1058 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 1080 | 1084 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 1195 | 1199 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.176 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 634 | 638 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 892 | 896 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 994 | 998 | PF00917 | 0.543 |
DOC_USP7_MATH_2 | 141 | 147 | PF00917 | 0.449 |
DOC_USP7_UBL2_3 | 259 | 263 | PF12436 | 0.482 |
DOC_USP7_UBL2_3 | 7 | 11 | PF12436 | 0.618 |
DOC_USP7_UBL2_3 | 742 | 746 | PF12436 | 0.241 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.350 |
LIG_14-3-3_CanoR_1 | 1000 | 1005 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 1214 | 1222 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 1230 | 1238 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 162 | 167 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 211 | 216 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 222 | 230 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 249 | 255 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 366 | 371 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 382 | 387 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 463 | 469 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 534 | 540 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 599 | 604 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 663 | 670 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 684 | 689 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 736 | 744 | PF00244 | 0.233 |
LIG_14-3-3_CanoR_1 | 831 | 836 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 897 | 903 | PF00244 | 0.432 |
LIG_BRCT_BRCA1_1 | 1048 | 1052 | PF00533 | 0.449 |
LIG_BRCT_BRCA1_1 | 464 | 468 | PF00533 | 0.490 |
LIG_BRCT_BRCA1_1 | 653 | 657 | PF00533 | 0.620 |
LIG_BRCT_BRCA1_1 | 784 | 788 | PF00533 | 0.490 |
LIG_Clathr_ClatBox_1 | 1186 | 1190 | PF01394 | 0.441 |
LIG_deltaCOP1_diTrp_1 | 647 | 657 | PF00928 | 0.606 |
LIG_EH1_1 | 750 | 758 | PF00400 | 0.307 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.291 |
LIG_FHA_1 | 1083 | 1089 | PF00498 | 0.544 |
LIG_FHA_1 | 1139 | 1145 | PF00498 | 0.428 |
LIG_FHA_1 | 1191 | 1197 | PF00498 | 0.436 |
LIG_FHA_1 | 1217 | 1223 | PF00498 | 0.508 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.451 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.157 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.206 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.445 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.383 |
LIG_FHA_1 | 778 | 784 | PF00498 | 0.432 |
LIG_FHA_1 | 808 | 814 | PF00498 | 0.412 |
LIG_FHA_1 | 857 | 863 | PF00498 | 0.322 |
LIG_FHA_2 | 1001 | 1007 | PF00498 | 0.394 |
LIG_FHA_2 | 1098 | 1104 | PF00498 | 0.498 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.582 |
LIG_FHA_2 | 1116 | 1122 | PF00498 | 0.416 |
LIG_FHA_2 | 1129 | 1135 | PF00498 | 0.418 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.478 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.575 |
LIG_FHA_2 | 465 | 471 | PF00498 | 0.432 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.355 |
LIG_FHA_2 | 587 | 593 | PF00498 | 0.514 |
LIG_FHA_2 | 677 | 683 | PF00498 | 0.567 |
LIG_FHA_2 | 795 | 801 | PF00498 | 0.514 |
LIG_FHA_2 | 952 | 958 | PF00498 | 0.262 |
LIG_GBD_Chelix_1 | 285 | 293 | PF00786 | 0.263 |
LIG_Integrin_isoDGR_2 | 597 | 599 | PF01839 | 0.361 |
LIG_IRF3_LxIS_1 | 719 | 726 | PF10401 | 0.164 |
LIG_LIR_Apic_2 | 1033 | 1037 | PF02991 | 0.419 |
LIG_LIR_Apic_2 | 369 | 373 | PF02991 | 0.562 |
LIG_LIR_Apic_2 | 621 | 627 | PF02991 | 0.761 |
LIG_LIR_Apic_2 | 797 | 802 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 1092 | 1099 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 248 | 255 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 307 | 316 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 42 | 52 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 465 | 474 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 589 | 596 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 60 | 70 | PF02991 | 0.250 |
LIG_LIR_Gen_1 | 665 | 675 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 699 | 709 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 785 | 792 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 84 | 94 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 960 | 971 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 1013 | 1019 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 1092 | 1098 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 194 | 198 | PF02991 | 0.164 |
LIG_LIR_Nem_3 | 307 | 311 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 465 | 471 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 589 | 593 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 620 | 626 | PF02991 | 0.696 |
LIG_LIR_Nem_3 | 661 | 667 | PF02991 | 0.698 |
LIG_LIR_Nem_3 | 698 | 704 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 769 | 775 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 785 | 791 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 960 | 966 | PF02991 | 0.237 |
LIG_NRBOX | 284 | 290 | PF00104 | 0.164 |
LIG_NRBOX | 753 | 759 | PF00104 | 0.209 |
LIG_NRBOX | 782 | 788 | PF00104 | 0.564 |
LIG_NRBOX | 808 | 814 | PF00104 | 0.449 |
LIG_PCNA_PIPBox_1 | 28 | 37 | PF02747 | 0.465 |
LIG_PCNA_yPIPBox_3 | 28 | 38 | PF02747 | 0.544 |
LIG_PDZ_Class_1 | 1263 | 1268 | PF00595 | 0.462 |
LIG_Pex14_2 | 1211 | 1215 | PF04695 | 0.581 |
LIG_Pex14_2 | 181 | 185 | PF04695 | 0.261 |
LIG_Pex14_2 | 63 | 67 | PF04695 | 0.282 |
LIG_PTB_Apo_2 | 1028 | 1035 | PF02174 | 0.402 |
LIG_PTB_Apo_2 | 364 | 371 | PF02174 | 0.517 |
LIG_PTB_Apo_2 | 669 | 676 | PF02174 | 0.464 |
LIG_PTB_Apo_2 | 69 | 76 | PF02174 | 0.334 |
LIG_PTB_Phospho_1 | 69 | 75 | PF10480 | 0.314 |
LIG_SH2_CRK | 1016 | 1020 | PF00017 | 0.521 |
LIG_SH2_CRK | 37 | 41 | PF00017 | 0.440 |
LIG_SH2_CRK | 751 | 755 | PF00017 | 0.314 |
LIG_SH2_CRK | 772 | 776 | PF00017 | 0.386 |
LIG_SH2_CRK | 87 | 91 | PF00017 | 0.155 |
LIG_SH2_CRK | 912 | 916 | PF00017 | 0.514 |
LIG_SH2_GRB2like | 667 | 670 | PF00017 | 0.478 |
LIG_SH2_NCK_1 | 1125 | 1129 | PF00017 | 0.474 |
LIG_SH2_NCK_1 | 220 | 224 | PF00017 | 0.474 |
LIG_SH2_NCK_1 | 667 | 671 | PF00017 | 0.540 |
LIG_SH2_SRC | 1014 | 1017 | PF00017 | 0.540 |
LIG_SH2_SRC | 423 | 426 | PF00017 | 0.355 |
LIG_SH2_SRC | 624 | 627 | PF00017 | 0.610 |
LIG_SH2_STAP1 | 1155 | 1159 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 491 | 495 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 590 | 594 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.226 |
LIG_SH2_STAP1 | 751 | 755 | PF00017 | 0.259 |
LIG_SH2_STAP1 | 87 | 91 | PF00017 | 0.166 |
LIG_SH2_STAT3 | 1161 | 1164 | PF00017 | 0.471 |
LIG_SH2_STAT3 | 292 | 295 | PF00017 | 0.155 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 624 | 627 | PF00017 | 0.702 |
LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 762 | 765 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 774 | 777 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 778 | 781 | PF00017 | 0.514 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.561 |
LIG_Sin3_3 | 513 | 520 | PF02671 | 0.504 |
LIG_SUMO_SIM_anti_2 | 1094 | 1100 | PF11976 | 0.460 |
LIG_SUMO_SIM_anti_2 | 1103 | 1109 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 1232 | 1240 | PF11976 | 0.496 |
LIG_SUMO_SIM_anti_2 | 186 | 191 | PF11976 | 0.241 |
LIG_SUMO_SIM_anti_2 | 307 | 313 | PF11976 | 0.383 |
LIG_SUMO_SIM_anti_2 | 405 | 412 | PF11976 | 0.474 |
LIG_SUMO_SIM_anti_2 | 521 | 527 | PF11976 | 0.431 |
LIG_SUMO_SIM_anti_2 | 937 | 944 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 1185 | 1191 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 1232 | 1240 | PF11976 | 0.515 |
LIG_SUMO_SIM_par_1 | 482 | 489 | PF11976 | 0.355 |
LIG_SUMO_SIM_par_1 | 521 | 527 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 926 | 931 | PF11976 | 0.355 |
LIG_TRAF2_1 | 1130 | 1133 | PF00917 | 0.442 |
LIG_TRAF2_1 | 467 | 470 | PF00917 | 0.475 |
LIG_TRAF2_1 | 589 | 592 | PF00917 | 0.429 |
LIG_TRFH_1 | 623 | 627 | PF08558 | 0.521 |
LIG_UBA3_1 | 1252 | 1260 | PF00899 | 0.274 |
LIG_UBA3_1 | 842 | 851 | PF00899 | 0.309 |
LIG_WRC_WIRS_1 | 237 | 242 | PF05994 | 0.247 |
LIG_WRC_WIRS_1 | 325 | 330 | PF05994 | 0.351 |
LIG_WRC_WIRS_1 | 899 | 904 | PF05994 | 0.285 |
MOD_CK1_1 | 1082 | 1088 | PF00069 | 0.164 |
MOD_CK1_1 | 1113 | 1119 | PF00069 | 0.337 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.389 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.341 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.264 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.275 |
MOD_CK1_1 | 551 | 557 | PF00069 | 0.415 |
MOD_CK1_1 | 637 | 643 | PF00069 | 0.689 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.558 |
MOD_CK1_1 | 665 | 671 | PF00069 | 0.538 |
MOD_CK1_1 | 711 | 717 | PF00069 | 0.239 |
MOD_CK1_1 | 895 | 901 | PF00069 | 0.363 |
MOD_CK1_1 | 931 | 937 | PF00069 | 0.164 |
MOD_CK1_1 | 986 | 992 | PF00069 | 0.605 |
MOD_CK2_1 | 1128 | 1134 | PF00069 | 0.297 |
MOD_CK2_1 | 1195 | 1201 | PF00069 | 0.400 |
MOD_CK2_1 | 1258 | 1264 | PF00069 | 0.385 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.475 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.347 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.351 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.301 |
MOD_CK2_1 | 464 | 470 | PF00069 | 0.277 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.427 |
MOD_CK2_1 | 580 | 586 | PF00069 | 0.370 |
MOD_CK2_1 | 676 | 682 | PF00069 | 0.475 |
MOD_CK2_1 | 951 | 957 | PF00069 | 0.305 |
MOD_Cter_Amidation | 137 | 140 | PF01082 | 0.179 |
MOD_Cter_Amidation | 461 | 464 | PF01082 | 0.263 |
MOD_GlcNHglycan | 1082 | 1085 | PF01048 | 0.330 |
MOD_GlcNHglycan | 1115 | 1118 | PF01048 | 0.271 |
MOD_GlcNHglycan | 1166 | 1169 | PF01048 | 0.266 |
MOD_GlcNHglycan | 1193 | 1196 | PF01048 | 0.374 |
MOD_GlcNHglycan | 1239 | 1242 | PF01048 | 0.479 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.330 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.559 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.406 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.379 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.303 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.249 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.271 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.242 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.271 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.391 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.426 |
MOD_GlcNHglycan | 813 | 816 | PF01048 | 0.309 |
MOD_GlcNHglycan | 882 | 885 | PF01048 | 0.379 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.447 |
MOD_GSK3_1 | 1191 | 1198 | PF00069 | 0.388 |
MOD_GSK3_1 | 1225 | 1232 | PF00069 | 0.416 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.324 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.297 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.330 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.434 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.676 |
MOD_GSK3_1 | 807 | 814 | PF00069 | 0.213 |
MOD_GSK3_1 | 827 | 834 | PF00069 | 0.330 |
MOD_GSK3_1 | 880 | 887 | PF00069 | 0.270 |
MOD_GSK3_1 | 937 | 944 | PF00069 | 0.376 |
MOD_GSK3_1 | 971 | 978 | PF00069 | 0.434 |
MOD_N-GLC_1 | 1030 | 1035 | PF02516 | 0.392 |
MOD_N-GLC_1 | 1046 | 1051 | PF02516 | 0.146 |
MOD_N-GLC_1 | 1215 | 1220 | PF02516 | 0.221 |
MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.417 |
MOD_N-GLC_1 | 958 | 963 | PF02516 | 0.164 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.371 |
MOD_NEK2_1 | 1061 | 1066 | PF00069 | 0.279 |
MOD_NEK2_1 | 1115 | 1120 | PF00069 | 0.284 |
MOD_NEK2_1 | 1215 | 1220 | PF00069 | 0.399 |
MOD_NEK2_1 | 1237 | 1242 | PF00069 | 0.454 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.361 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.340 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.299 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.164 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.400 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.396 |
MOD_NEK2_1 | 694 | 699 | PF00069 | 0.407 |
MOD_NEK2_1 | 708 | 713 | PF00069 | 0.248 |
MOD_NEK2_1 | 723 | 728 | PF00069 | 0.246 |
MOD_NEK2_1 | 863 | 868 | PF00069 | 0.266 |
MOD_NEK2_1 | 941 | 946 | PF00069 | 0.301 |
MOD_NEK2_1 | 971 | 976 | PF00069 | 0.323 |
MOD_NEK2_2 | 892 | 897 | PF00069 | 0.420 |
MOD_PIKK_1 | 442 | 448 | PF00454 | 0.271 |
MOD_PIKK_1 | 497 | 503 | PF00454 | 0.285 |
MOD_PIKK_1 | 545 | 551 | PF00454 | 0.404 |
MOD_PIKK_1 | 662 | 668 | PF00454 | 0.616 |
MOD_PIKK_1 | 723 | 729 | PF00454 | 0.386 |
MOD_PIKK_1 | 735 | 741 | PF00454 | 0.386 |
MOD_PK_1 | 211 | 217 | PF00069 | 0.164 |
MOD_PK_1 | 382 | 388 | PF00069 | 0.225 |
MOD_PK_1 | 684 | 690 | PF00069 | 0.421 |
MOD_PK_1 | 831 | 837 | PF00069 | 0.263 |
MOD_PKA_1 | 684 | 690 | PF00069 | 0.381 |
MOD_PKA_2 | 1224 | 1230 | PF00069 | 0.386 |
MOD_PKA_2 | 1245 | 1251 | PF00069 | 0.400 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.346 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.368 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.318 |
MOD_PKA_2 | 462 | 468 | PF00069 | 0.386 |
MOD_PKA_2 | 533 | 539 | PF00069 | 0.418 |
MOD_PKA_2 | 662 | 668 | PF00069 | 0.476 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.396 |
MOD_PKA_2 | 683 | 689 | PF00069 | 0.377 |
MOD_PKA_2 | 735 | 741 | PF00069 | 0.391 |
MOD_PKA_2 | 880 | 886 | PF00069 | 0.391 |
MOD_PKA_2 | 994 | 1000 | PF00069 | 0.466 |
MOD_Plk_1 | 1030 | 1036 | PF00069 | 0.360 |
MOD_Plk_1 | 1046 | 1052 | PF00069 | 0.306 |
MOD_Plk_1 | 1091 | 1097 | PF00069 | 0.361 |
MOD_Plk_1 | 1215 | 1221 | PF00069 | 0.321 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.164 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.298 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.531 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.395 |
MOD_Plk_1 | 619 | 625 | PF00069 | 0.697 |
MOD_Plk_1 | 646 | 652 | PF00069 | 0.658 |
MOD_Plk_1 | 794 | 800 | PF00069 | 0.228 |
MOD_Plk_1 | 937 | 943 | PF00069 | 0.386 |
MOD_Plk_1 | 958 | 964 | PF00069 | 0.218 |
MOD_Plk_2-3 | 1097 | 1103 | PF00069 | 0.291 |
MOD_Plk_2-3 | 533 | 539 | PF00069 | 0.418 |
MOD_Plk_2-3 | 586 | 592 | PF00069 | 0.377 |
MOD_Plk_2-3 | 676 | 682 | PF00069 | 0.386 |
MOD_Plk_4 | 1067 | 1073 | PF00069 | 0.320 |
MOD_Plk_4 | 1082 | 1088 | PF00069 | 0.320 |
MOD_Plk_4 | 1091 | 1097 | PF00069 | 0.306 |
MOD_Plk_4 | 1103 | 1109 | PF00069 | 0.265 |
MOD_Plk_4 | 1110 | 1116 | PF00069 | 0.231 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.386 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.315 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.369 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.255 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.307 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.271 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.281 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.377 |
MOD_Plk_4 | 580 | 586 | PF00069 | 0.372 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.435 |
MOD_Plk_4 | 619 | 625 | PF00069 | 0.388 |
MOD_Plk_4 | 686 | 692 | PF00069 | 0.444 |
MOD_Plk_4 | 708 | 714 | PF00069 | 0.262 |
MOD_Plk_4 | 794 | 800 | PF00069 | 0.249 |
MOD_Plk_4 | 808 | 814 | PF00069 | 0.322 |
MOD_Plk_4 | 863 | 869 | PF00069 | 0.297 |
MOD_Plk_4 | 884 | 890 | PF00069 | 0.299 |
MOD_Plk_4 | 945 | 951 | PF00069 | 0.261 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.325 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.459 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.350 |
MOD_SUMO_rev_2 | 3 | 8 | PF00179 | 0.551 |
MOD_SUMO_rev_2 | 527 | 536 | PF00179 | 0.396 |
MOD_SUMO_rev_2 | 680 | 687 | PF00179 | 0.515 |
TRG_AP2beta_CARGO_1 | 1092 | 1102 | PF09066 | 0.164 |
TRG_DiLeu_BaEn_1 | 186 | 191 | PF01217 | 0.295 |
TRG_DiLeu_BaEn_1 | 782 | 787 | PF01217 | 0.164 |
TRG_DiLeu_BaLyEn_6 | 193 | 198 | PF01217 | 0.271 |
TRG_ENDOCYTIC_2 | 1016 | 1019 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 590 | 593 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 667 | 670 | PF00928 | 0.590 |
TRG_ENDOCYTIC_2 | 751 | 754 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 772 | 775 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 912 | 915 | PF00928 | 0.274 |
TRG_ER_diArg_1 | 1213 | 1215 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 437 | 440 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 802 | 804 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 925 | 927 | PF00400 | 0.218 |
TRG_NLS_MonoExtC_3 | 909 | 914 | PF00514 | 0.202 |
TRG_NLS_MonoExtN_4 | 907 | 914 | PF00514 | 0.202 |
TRG_Pf-PMV_PEXEL_1 | 382 | 387 | PF00026 | 0.243 |
TRG_Pf-PMV_PEXEL_1 | 542 | 546 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 784 | 789 | PF00026 | 0.164 |
TRG_Pf-PMV_PEXEL_1 | 790 | 794 | PF00026 | 0.154 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A059JJ46 | Trichophyton interdigitale (strain MR816) | 32% | 95% |
A0A059JK44 | Trichophyton interdigitale (strain MR816) | 28% | 92% |
A0A095C325 | Cryptococcus gattii serotype B (strain R265) | 33% | 90% |
A0A0D1BUH6 | Ustilago maydis (strain 521 / FGSC 9021) | 29% | 92% |
A0A0D1CZ63 | Ustilago maydis (strain 521 / FGSC 9021) | 25% | 95% |
A0A0N0P6R0 | Leptomonas seymouri | 46% | 92% |
A0A0N1IM38 | Leptomonas seymouri | 71% | 100% |
A0A0S4IJN7 | Bodo saltans | 24% | 100% |
A0A0S4IRS2 | Bodo saltans | 46% | 100% |
A0A0S4JDP8 | Bodo saltans | 46% | 100% |
A0A0S4JGM3 | Bodo saltans | 48% | 100% |
A0A0U1LQE1 | Talaromyces islandicus | 26% | 82% |
A0A1U8QG99 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 30% | 99% |
A0A1U9YI12 | Clonostachys rogersoniana | 29% | 100% |
A0A1X0P748 | Trypanosomatidae | 44% | 100% |
A0A1X0P9E7 | Trypanosomatidae | 47% | 99% |
A0A348AXX9 | Curvularia clavata | 30% | 95% |
A0A3Q8ICF5 | Leishmania donovani | 85% | 100% |
A0A3S7X7M2 | Leishmania donovani | 47% | 95% |
A2XCD4 | Oryza sativa subsp. indica | 25% | 84% |
A4I2J3 | Leishmania infantum | 85% | 100% |
A4I9R3 | Leishmania infantum | 46% | 95% |
A7A063 | Saccharomyces cerevisiae (strain YJM789) | 22% | 81% |
A7KVC2 | Zea mays | 25% | 84% |
B2KWH4 | Ajellomyces capsulatus | 29% | 96% |
B2RX12 | Mus musculus | 24% | 83% |
B5X0E4 | Mus musculus | 33% | 100% |
B8K1W2 | Canis lupus familiaris | 34% | 96% |
C9ZMP2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 84% |
E9AYP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
E9B4S1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 95% |
F2PRR1 | Trichophyton equinum (strain ATCC MYA-4606 / CBS 127.97) | 32% | 95% |
F2Q5G0 | Trichophyton equinum (strain ATCC MYA-4606 / CBS 127.97) | 28% | 92% |
F2RP52 | Trichophyton tonsurans (strain CBS 112818) | 32% | 95% |
F2RPA4 | Trichophyton tonsurans (strain CBS 112818) | 27% | 93% |
F2SQT8 | Trichophyton rubrum (strain ATCC MYA-4607 / CBS 118892) | 30% | 98% |
F2T1C4 | Trichophyton rubrum (strain ATCC MYA-4607 / CBS 118892) | 32% | 95% |
G5EE72 | Caenorhabditis elegans | 23% | 89% |
H6TB12 | Starmerella bombicola | 31% | 98% |
J9VF33 | Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) | 33% | 90% |
O15439 | Homo sapiens | 26% | 96% |
O35379 | Mus musculus | 25% | 83% |
O70127 | Rattus norvegicus | 34% | 96% |
O80725 | Arabidopsis thaliana | 33% | 99% |
O88563 | Rattus norvegicus | 25% | 83% |
O95255 | Homo sapiens | 24% | 84% |
O95342 | Homo sapiens | 34% | 96% |
P06795 | Mus musculus | 35% | 99% |
P08183 | Homo sapiens | 36% | 99% |
P0CU83 | Trichophyton rubrum (strain ATCC MYA-4607 / CBS 118892) | 28% | 93% |
P12866 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 98% |
P13568 | Plasmodium falciparum (isolate FC27 / Papua New Guinea) | 26% | 89% |
P21439 | Homo sapiens | 35% | 99% |
P21440 | Mus musculus | 35% | 99% |
P21447 | Mus musculus | 35% | 99% |
P21448 | Cricetulus griseus | 35% | 99% |
P21449 | Cricetulus griseus | 35% | 99% |
P23174 | Cricetulus griseus | 35% | 99% |
P33527 | Homo sapiens | 26% | 83% |
P34712 | Caenorhabditis elegans | 31% | 96% |
P34713 | Caenorhabditis elegans | 32% | 100% |
P36619 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 93% |
P43245 | Rattus norvegicus | 35% | 99% |
P53049 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 86% |
P53706 | Candida albicans (strain WO-1) | 22% | 96% |
P78966 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 95% |
P91660 | Drosophila melanogaster | 24% | 92% |
Q00748 | Drosophila melanogaster | 30% | 97% |
Q06034 | Leishmania enriettii | 47% | 99% |
Q08201 | Rattus norvegicus | 35% | 99% |
Q09427 | Cricetus cricetus | 26% | 80% |
Q09428 | Homo sapiens | 25% | 80% |
Q10RX7 | Oryza sativa subsp. japonica | 25% | 84% |
Q2M3G0 | Homo sapiens | 33% | 100% |
Q42093 | Arabidopsis thaliana | 25% | 78% |
Q4Q3A6 | Leishmania major | 46% | 100% |
Q4Q8S4 | Leishmania major | 84% | 100% |
Q4WA92 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 31% | 100% |
Q4WD46 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 32% | 99% |
Q4WSI1 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 28% | 95% |
Q4WTT9 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 32% | 94% |
Q54BT3 | Dictyostelium discoideum | 34% | 91% |
Q54JR2 | Dictyostelium discoideum | 23% | 90% |
Q54V86 | Dictyostelium discoideum | 26% | 94% |
Q5A762 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 24% | 79% |
Q5AV01 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 23% | 81% |
Q5BAY0 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 33% | 94% |
Q5F364 | Gallus gallus | 24% | 83% |
Q6FWS5 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 23% | 77% |
Q6Q876 | Leptosphaeria maculans | 31% | 100% |
Q6UR05 | Canis lupus familiaris | 25% | 83% |
Q6Y306 | Rattus norvegicus | 24% | 93% |
Q6YUU5 | Oryza sativa subsp. japonica | 32% | 100% |
Q7DM58 | Arabidopsis thaliana | 25% | 84% |
Q864R9 | Macaca fascicularis | 24% | 83% |
Q8CG09 | Rattus norvegicus | 24% | 83% |
Q8HXQ5 | Bos taurus | 26% | 83% |
Q8LPK2 | Arabidopsis thaliana | 32% | 100% |
Q8T9W4 | Dictyostelium discoideum | 32% | 89% |
Q8VZZ4 | Arabidopsis thaliana | 25% | 86% |
Q96J66 | Homo sapiens | 23% | 92% |
Q9C7F2 | Arabidopsis thaliana | 32% | 100% |
Q9C7F8 | Arabidopsis thaliana | 32% | 100% |
Q9C8G9 | Arabidopsis thaliana | 26% | 78% |
Q9C8H0 | Arabidopsis thaliana | 25% | 85% |
Q9C8H1 | Arabidopsis thaliana | 25% | 85% |
Q9FHF1 | Arabidopsis thaliana | 32% | 100% |
Q9FWX7 | Arabidopsis thaliana | 34% | 99% |
Q9FWX8 | Arabidopsis thaliana | 32% | 100% |
Q9LHD1 | Arabidopsis thaliana | 30% | 100% |
Q9LHK4 | Arabidopsis thaliana | 30% | 100% |
Q9LJX0 | Arabidopsis thaliana | 33% | 100% |
Q9LK64 | Arabidopsis thaliana | 25% | 84% |
Q9LSJ2 | Arabidopsis thaliana | 31% | 100% |
Q9LSJ5 | Arabidopsis thaliana | 32% | 100% |
Q9LSJ6 | Arabidopsis thaliana | 32% | 100% |
Q9LSJ8 | Arabidopsis thaliana | 32% | 100% |
Q9LZJ5 | Arabidopsis thaliana | 23% | 82% |
Q9M0M2 | Arabidopsis thaliana | 33% | 100% |
Q9M1C7 | Arabidopsis thaliana | 25% | 84% |
Q9M1Q9 | Arabidopsis thaliana | 34% | 98% |
Q9N0V3 | Oryctolagus cuniculus | 33% | 96% |
Q9P5N0 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 87% |
Q9QY30 | Mus musculus | 34% | 96% |
Q9R1S7 | Mus musculus | 25% | 85% |
Q9SGY1 | Arabidopsis thaliana | 33% | 100% |
Q9SYI2 | Arabidopsis thaliana | 33% | 100% |
Q9SYI3 | Arabidopsis thaliana | 33% | 100% |
Q9Y8G1 | Emericella nidulans | 33% | 94% |
Q9Y8G2 | Emericella nidulans | 30% | 99% |
Q9ZR72 | Arabidopsis thaliana | 32% | 99% |
S0EGU4 | Gibberella fujikuroi (strain CBS 195.34 / IMI 58289 / NRRL A-6831) | 28% | 97% |
S3D778 | Glarea lozoyensis (strain ATCC 20868 / MF5171) | 25% | 96% |