Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A0A3Q8IGY9
Term | Name | Level | Count |
---|---|---|---|
GO:0042592 | homeostatic process | 3 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 1 |
GO:0055070 | copper ion homeostasis | 9 | 1 |
GO:0055076 | obsolete transition metal ion homeostasis | 8 | 1 |
GO:0055080 | monoatomic cation homeostasis | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005215 | transporter activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005507 | copper ion binding | 6 | 5 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 11 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 11 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 11 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 11 |
GO:0022804 | active transmembrane transporter activity | 3 | 11 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 11 |
GO:0022857 | transmembrane transporter activity | 2 | 11 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0046914 | transition metal ion binding | 5 | 5 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0005375 | copper ion transmembrane transporter activity | 7 | 1 |
GO:0015662 | P-type ion transporter activity | 4 | 1 |
GO:0043682 | P-type divalent copper transporter activity | 4 | 1 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 1 |
GO:0046915 | transition metal ion transmembrane transporter activity | 6 | 1 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1068 | 1072 | PF00656 | 0.499 |
CLV_C14_Caspase3-7 | 61 | 65 | PF00656 | 0.526 |
CLV_C14_Caspase3-7 | 966 | 970 | PF00656 | 0.435 |
CLV_NRD_NRD_1 | 1094 | 1096 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 874 | 876 | PF00675 | 0.270 |
CLV_PCSK_FUR_1 | 158 | 162 | PF00082 | 0.502 |
CLV_PCSK_FUR_1 | 566 | 570 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 1094 | 1096 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 874 | 876 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 972 | 974 | PF00082 | 0.291 |
CLV_PCSK_PC1ET2_1 | 568 | 570 | PF00082 | 0.312 |
CLV_PCSK_PC1ET2_1 | 972 | 974 | PF00082 | 0.291 |
CLV_PCSK_PC7_1 | 12 | 18 | PF00082 | 0.360 |
CLV_PCSK_PC7_1 | 218 | 224 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 1036 | 1040 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.218 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 471 | 475 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 542 | 546 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 605 | 609 | PF00082 | 0.334 |
CLV_Separin_Metazoa | 808 | 812 | PF03568 | 0.492 |
DEG_APCC_DBOX_1 | 332 | 340 | PF00400 | 0.588 |
DEG_APCC_DBOX_1 | 470 | 478 | PF00400 | 0.312 |
DEG_SPOP_SBC_1 | 1142 | 1146 | PF00917 | 0.365 |
DEG_SPOP_SBC_1 | 822 | 826 | PF00917 | 0.434 |
DOC_ANK_TNKS_1 | 615 | 622 | PF00023 | 0.425 |
DOC_CKS1_1 | 485 | 490 | PF01111 | 0.326 |
DOC_CKS1_1 | 759 | 764 | PF01111 | 0.429 |
DOC_CYCLIN_yCln2_LP_2 | 1117 | 1123 | PF00134 | 0.481 |
DOC_CYCLIN_yCln2_LP_2 | 286 | 292 | PF00134 | 0.435 |
DOC_CYCLIN_yCln2_LP_2 | 452 | 458 | PF00134 | 0.271 |
DOC_MAPK_FxFP_2 | 536 | 539 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 16 | 22 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 222 | 229 | PF00069 | 0.739 |
DOC_MAPK_gen_1 | 266 | 276 | PF00069 | 0.375 |
DOC_MAPK_MEF2A_6 | 269 | 278 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 471 | 478 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 984 | 991 | PF00069 | 0.448 |
DOC_MAPK_RevD_3 | 1080 | 1095 | PF00069 | 0.477 |
DOC_PP1_RVXF_1 | 1034 | 1040 | PF00149 | 0.476 |
DOC_PP2B_LxvP_1 | 1109 | 1112 | PF13499 | 0.368 |
DOC_PP2B_LxvP_1 | 452 | 455 | PF13499 | 0.331 |
DOC_PP2B_LxvP_1 | 819 | 822 | PF13499 | 0.375 |
DOC_PP4_FxxP_1 | 536 | 539 | PF00568 | 0.393 |
DOC_USP7_MATH_1 | 1112 | 1116 | PF00917 | 0.296 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 733 | 737 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 829 | 833 | PF00917 | 0.547 |
DOC_WW_Pin1_4 | 1044 | 1049 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.290 |
DOC_WW_Pin1_4 | 758 | 763 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.784 |
LIG_14-3-3_CanoR_1 | 16 | 21 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 218 | 226 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 230 | 234 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 542 | 547 | PF00244 | 0.275 |
LIG_14-3-3_CanoR_1 | 566 | 576 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 597 | 603 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 697 | 703 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 898 | 907 | PF00244 | 0.375 |
LIG_APCC_ABBA_1 | 462 | 467 | PF00400 | 0.329 |
LIG_BIR_III_2 | 724 | 728 | PF00653 | 0.510 |
LIG_BRCT_BRCA1_1 | 155 | 159 | PF00533 | 0.714 |
LIG_BRCT_BRCA1_1 | 274 | 278 | PF00533 | 0.510 |
LIG_CaM_IQ_9 | 1082 | 1097 | PF13499 | 0.464 |
LIG_CtBP_PxDLS_1 | 637 | 642 | PF00389 | 0.435 |
LIG_deltaCOP1_diTrp_1 | 734 | 744 | PF00928 | 0.491 |
LIG_EH1_1 | 509 | 517 | PF00400 | 0.474 |
LIG_eIF4E_1 | 510 | 516 | PF01652 | 0.555 |
LIG_FHA_1 | 1142 | 1148 | PF00498 | 0.398 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.546 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.634 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.709 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.515 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.649 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.718 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.472 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.268 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.445 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.296 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.451 |
LIG_FHA_1 | 652 | 658 | PF00498 | 0.439 |
LIG_FHA_1 | 711 | 717 | PF00498 | 0.514 |
LIG_FHA_1 | 797 | 803 | PF00498 | 0.437 |
LIG_FHA_1 | 810 | 816 | PF00498 | 0.429 |
LIG_FHA_1 | 867 | 873 | PF00498 | 0.539 |
LIG_FHA_1 | 933 | 939 | PF00498 | 0.467 |
LIG_FHA_1 | 949 | 955 | PF00498 | 0.376 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.672 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.596 |
LIG_FHA_2 | 543 | 549 | PF00498 | 0.271 |
LIG_FHA_2 | 620 | 626 | PF00498 | 0.453 |
LIG_FHA_2 | 781 | 787 | PF00498 | 0.545 |
LIG_Integrin_isoDGR_2 | 804 | 806 | PF01839 | 0.296 |
LIG_LIR_Apic_2 | 534 | 539 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 275 | 286 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 463 | 473 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 523 | 533 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 554 | 563 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 734 | 745 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 156 | 162 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 463 | 468 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 523 | 529 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 554 | 559 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 701 | 705 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 734 | 740 | PF02991 | 0.518 |
LIG_LYPXL_S_1 | 1118 | 1122 | PF13949 | 0.382 |
LIG_LYPXL_SIV_4 | 525 | 533 | PF13949 | 0.280 |
LIG_MAD2 | 610 | 618 | PF02301 | 0.416 |
LIG_MYND_1 | 105 | 109 | PF01753 | 0.680 |
LIG_NRBOX | 1078 | 1084 | PF00104 | 0.465 |
LIG_NRBOX | 715 | 721 | PF00104 | 0.454 |
LIG_Pex14_1 | 1102 | 1106 | PF04695 | 0.271 |
LIG_Pex14_2 | 1100 | 1104 | PF04695 | 0.271 |
LIG_Pex14_2 | 155 | 159 | PF04695 | 0.664 |
LIG_Pex14_2 | 493 | 497 | PF04695 | 0.256 |
LIG_Pex14_2 | 498 | 502 | PF04695 | 0.318 |
LIG_Pex14_2 | 705 | 709 | PF04695 | 0.510 |
LIG_Pex14_2 | 740 | 744 | PF04695 | 0.419 |
LIG_REV1ctd_RIR_1 | 1119 | 1126 | PF16727 | 0.419 |
LIG_SH2_CRK | 1106 | 1110 | PF00017 | 0.296 |
LIG_SH2_CRK | 526 | 530 | PF00017 | 0.331 |
LIG_SH2_SRC | 1015 | 1018 | PF00017 | 0.435 |
LIG_SH2_SRC | 524 | 527 | PF00017 | 0.271 |
LIG_SH2_STAP1 | 1015 | 1019 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 350 | 354 | PF00017 | 0.587 |
LIG_SH2_STAP1 | 526 | 530 | PF00017 | 0.384 |
LIG_SH2_STAT3 | 80 | 83 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 981 | 984 | PF00017 | 0.472 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.510 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.196 |
LIG_SH3_3 | 908 | 914 | PF00018 | 0.451 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.794 |
LIG_SH3_4 | 688 | 695 | PF00018 | 0.416 |
LIG_SUMO_SIM_anti_2 | 1077 | 1084 | PF11976 | 0.462 |
LIG_SUMO_SIM_anti_2 | 1138 | 1146 | PF11976 | 0.296 |
LIG_SUMO_SIM_par_1 | 1107 | 1113 | PF11976 | 0.268 |
LIG_SUMO_SIM_par_1 | 178 | 186 | PF11976 | 0.642 |
LIG_SUMO_SIM_par_1 | 513 | 520 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 574 | 580 | PF11976 | 0.572 |
LIG_SUMO_SIM_par_1 | 963 | 969 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 988 | 993 | PF11976 | 0.429 |
LIG_TRAF2_1 | 646 | 649 | PF00917 | 0.453 |
LIG_TRAF2_1 | 784 | 787 | PF00917 | 0.477 |
LIG_UBA3_1 | 1082 | 1090 | PF00899 | 0.456 |
LIG_WRC_WIRS_1 | 553 | 558 | PF05994 | 0.296 |
LIG_WW_3 | 912 | 916 | PF00397 | 0.470 |
MOD_CDK_SPxxK_3 | 421 | 428 | PF00069 | 0.497 |
MOD_CK1_1 | 1089 | 1095 | PF00069 | 0.467 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.647 |
MOD_CK1_1 | 1138 | 1144 | PF00069 | 0.282 |
MOD_CK1_1 | 1145 | 1151 | PF00069 | 0.256 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.592 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.573 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.695 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.463 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.503 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.665 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.406 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.440 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.356 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.689 |
MOD_CK1_1 | 710 | 716 | PF00069 | 0.511 |
MOD_CK1_1 | 781 | 787 | PF00069 | 0.488 |
MOD_CK1_1 | 882 | 888 | PF00069 | 0.510 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.757 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.608 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.585 |
MOD_CK2_1 | 619 | 625 | PF00069 | 0.472 |
MOD_CK2_1 | 780 | 786 | PF00069 | 0.547 |
MOD_CMANNOS | 502 | 505 | PF00535 | 0.337 |
MOD_DYRK1A_RPxSP_1 | 201 | 205 | PF00069 | 0.584 |
MOD_DYRK1A_RPxSP_1 | 230 | 234 | PF00069 | 0.572 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.483 |
MOD_GlcNHglycan | 1114 | 1117 | PF01048 | 0.296 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.319 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.453 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.299 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.384 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.340 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.367 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.248 |
MOD_GlcNHglycan | 780 | 783 | PF01048 | 0.291 |
MOD_GlcNHglycan | 857 | 860 | PF01048 | 0.322 |
MOD_GlcNHglycan | 866 | 869 | PF01048 | 0.290 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.645 |
MOD_GSK3_1 | 1138 | 1145 | PF00069 | 0.291 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.571 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.726 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.707 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.679 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.511 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.604 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.489 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.431 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.448 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.299 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.396 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.322 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.284 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.515 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.418 |
MOD_GSK3_1 | 651 | 658 | PF00069 | 0.419 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.418 |
MOD_GSK3_1 | 796 | 803 | PF00069 | 0.416 |
MOD_GSK3_1 | 862 | 869 | PF00069 | 0.413 |
MOD_GSK3_1 | 878 | 885 | PF00069 | 0.437 |
MOD_LATS_1 | 540 | 546 | PF00433 | 0.235 |
MOD_N-GLC_1 | 1044 | 1049 | PF02516 | 0.247 |
MOD_N-GLC_1 | 191 | 196 | PF02516 | 0.394 |
MOD_N-GLC_1 | 276 | 281 | PF02516 | 0.270 |
MOD_N-GLC_1 | 655 | 660 | PF02516 | 0.216 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.755 |
MOD_NEK2_1 | 1135 | 1140 | PF00069 | 0.301 |
MOD_NEK2_1 | 1143 | 1148 | PF00069 | 0.290 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.449 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.510 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.472 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.427 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.494 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.495 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.267 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.227 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.422 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.334 |
MOD_NEK2_1 | 655 | 660 | PF00069 | 0.460 |
MOD_NEK2_1 | 707 | 712 | PF00069 | 0.451 |
MOD_NEK2_1 | 744 | 749 | PF00069 | 0.427 |
MOD_NEK2_1 | 766 | 771 | PF00069 | 0.416 |
MOD_NEK2_1 | 778 | 783 | PF00069 | 0.472 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.432 |
MOD_NEK2_1 | 796 | 801 | PF00069 | 0.480 |
MOD_NEK2_2 | 531 | 536 | PF00069 | 0.333 |
MOD_NEK2_2 | 893 | 898 | PF00069 | 0.375 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.635 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.637 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.600 |
MOD_PIKK_1 | 598 | 604 | PF00454 | 0.435 |
MOD_PKA_1 | 16 | 22 | PF00069 | 0.435 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.665 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.771 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.447 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.713 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.633 |
MOD_PKA_2 | 596 | 602 | PF00069 | 0.510 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.643 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.711 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.718 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.470 |
MOD_Plk_1 | 669 | 675 | PF00069 | 0.456 |
MOD_Plk_1 | 733 | 739 | PF00069 | 0.512 |
MOD_Plk_1 | 891 | 897 | PF00069 | 0.499 |
MOD_Plk_2-3 | 191 | 197 | PF00069 | 0.665 |
MOD_Plk_2-3 | 625 | 631 | PF00069 | 0.429 |
MOD_Plk_2-3 | 866 | 872 | PF00069 | 0.435 |
MOD_Plk_4 | 1075 | 1081 | PF00069 | 0.473 |
MOD_Plk_4 | 1138 | 1144 | PF00069 | 0.354 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.484 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.715 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.513 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.354 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.421 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.337 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.216 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.254 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.487 |
MOD_Plk_4 | 619 | 625 | PF00069 | 0.472 |
MOD_Plk_4 | 657 | 663 | PF00069 | 0.444 |
MOD_Plk_4 | 669 | 675 | PF00069 | 0.411 |
MOD_Plk_4 | 698 | 704 | PF00069 | 0.496 |
MOD_Plk_4 | 745 | 751 | PF00069 | 0.419 |
MOD_Plk_4 | 879 | 885 | PF00069 | 0.543 |
MOD_Plk_4 | 949 | 955 | PF00069 | 0.472 |
MOD_ProDKin_1 | 1044 | 1050 | PF00069 | 0.447 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.671 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.587 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.515 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.501 |
MOD_ProDKin_1 | 484 | 490 | PF00069 | 0.290 |
MOD_ProDKin_1 | 758 | 764 | PF00069 | 0.449 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.783 |
MOD_SUMO_for_1 | 1022 | 1025 | PF00179 | 0.375 |
MOD_SUMO_for_1 | 971 | 974 | PF00179 | 0.416 |
MOD_SUMO_rev_2 | 256 | 265 | PF00179 | 0.470 |
MOD_SUMO_rev_2 | 67 | 76 | PF00179 | 0.432 |
TRG_DiLeu_BaEn_1 | 184 | 189 | PF01217 | 0.732 |
TRG_DiLeu_BaEn_1 | 577 | 582 | PF01217 | 0.552 |
TRG_DiLeu_BaEn_1 | 937 | 942 | PF01217 | 0.470 |
TRG_DiLeu_BaEn_4 | 184 | 190 | PF01217 | 0.672 |
TRG_DiLeu_BaLyEn_6 | 469 | 474 | PF01217 | 0.453 |
TRG_DiLeu_LyEn_5 | 184 | 189 | PF01217 | 0.719 |
TRG_ENDOCYTIC_2 | 1097 | 1100 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 1106 | 1109 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 1119 | 1122 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 526 | 529 | PF00928 | 0.331 |
TRG_ER_diArg_1 | 1093 | 1095 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 157 | 159 | PF00400 | 0.670 |
TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 222 | 224 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 874 | 877 | PF00400 | 0.468 |
TRG_NES_CRM1_1 | 467 | 479 | PF08389 | 0.253 |
TRG_NES_CRM1_1 | 50 | 64 | PF08389 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 1028 | 1032 | PF00026 | 0.281 |
TRG_Pf-PMV_PEXEL_1 | 187 | 191 | PF00026 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 437 | 441 | PF00026 | 0.374 |
TRG_Pf-PMV_PEXEL_1 | 610 | 615 | PF00026 | 0.218 |
TRG_Pf-PMV_PEXEL_1 | 860 | 864 | PF00026 | 0.310 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFW0 | Leptomonas seymouri | 60% | 100% |
A0A0S4J742 | Bodo saltans | 40% | 100% |
A0A1X0P531 | Trypanosomatidae | 50% | 100% |
A0A422NN19 | Trypanosoma rangeli | 49% | 100% |
A3AWA4 | Oryza sativa subsp. japonica | 35% | 100% |
A4HLS1 | Leishmania braziliensis | 81% | 100% |
A4I980 | Leishmania infantum | 100% | 100% |
A5IVY3 | Staphylococcus aureus (strain JH9) | 35% | 100% |
A6QK47 | Staphylococcus aureus (strain Newman) | 35% | 100% |
A6U4T8 | Staphylococcus aureus (strain JH1) | 35% | 100% |
A7X6S1 | Staphylococcus aureus (strain Mu3 / ATCC 700698) | 35% | 100% |
A8Z3F8 | Staphylococcus aureus (strain USA300 / TCH1516) | 35% | 100% |
B9DFX7 | Arabidopsis thaliana | 29% | 100% |
D0A5R6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9B447 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
O29777 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 35% | 100% |
O32220 | Bacillus subtilis (strain 168) | 33% | 100% |
O59666 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
P35670 | Homo sapiens | 30% | 79% |
P37386 | Staphylococcus aureus | 26% | 100% |
P38995 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
P46839 | Mycobacterium leprae (strain TN) | 33% | 100% |
P49015 | Cricetulus griseus | 33% | 79% |
P58341 | Rhizobium meliloti (strain 1021) | 33% | 100% |
P58342 | Rhizobium meliloti (strain 1021) | 33% | 100% |
P70705 | Rattus norvegicus | 33% | 78% |
Q04656 | Homo sapiens | 34% | 78% |
Q2FDV0 | Staphylococcus aureus (strain USA300) | 35% | 100% |
Q2FV64 | Staphylococcus aureus (strain NCTC 8325 / PS 47) | 35% | 100% |
Q2YWA3 | Staphylococcus aureus (strain bovine RF122 / ET3-1) | 34% | 100% |
Q4A0G1 | Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM 20229 / NCIMB 8711 / NCTC 7292 / S-41) | 33% | 100% |
Q4L970 | Staphylococcus haemolyticus (strain JCSC1435) | 32% | 100% |
Q4Q3X8 | Leishmania major | 94% | 100% |
Q59385 | Escherichia coli (strain K12) | 33% | 100% |
Q5HCZ3 | Staphylococcus aureus (strain COL) | 35% | 100% |
Q5HL56 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 32% | 100% |
Q64430 | Mus musculus | 33% | 78% |
Q64446 | Mus musculus | 34% | 80% |
Q64535 | Rattus norvegicus | 33% | 80% |
Q6G6B7 | Staphylococcus aureus (strain MSSA476) | 35% | 100% |
Q6GDP1 | Staphylococcus aureus (strain MRSA252) | 35% | 100% |
Q6H7M3 | Oryza sativa subsp. japonica | 36% | 100% |
Q7A3E6 | Staphylococcus aureus (strain N315) | 35% | 100% |
Q8CN02 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 32% | 100% |
Q8NUQ9 | Staphylococcus aureus (strain MW2) | 35% | 100% |
Q8XD24 | Escherichia coli O157:H7 | 33% | 100% |
Q8Z8S4 | Salmonella typhi | 33% | 100% |
Q8ZCA7 | Yersinia pestis | 33% | 100% |
Q8ZR95 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 33% | 100% |
Q99R80 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 35% | 100% |
Q9KPZ7 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 32% | 100% |
Q9SH30 | Arabidopsis thaliana | 34% | 100% |
Q9SZC9 | Arabidopsis thaliana | 32% | 100% |
Q9X5X3 | Sinorhizobium medicae (strain WSM419) | 33% | 100% |
Q9XT50 | Ovis aries | 34% | 77% |