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: A4HLS1
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: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: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:0005507 | copper ion binding | 6 | 4 |
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:0046914 | transition metal ion binding | 5 | 4 |
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 | 1041 | 1045 | PF00656 | 0.506 |
CLV_C14_Caspase3-7 | 291 | 295 | PF00656 | 0.657 |
CLV_C14_Caspase3-7 | 372 | 376 | PF00656 | 0.375 |
CLV_C14_Caspase3-7 | 804 | 808 | PF00656 | 0.371 |
CLV_NRD_NRD_1 | 1067 | 1069 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 762 | 764 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 847 | 849 | PF00675 | 0.270 |
CLV_PCSK_FUR_1 | 134 | 138 | PF00082 | 0.510 |
CLV_PCSK_FUR_1 | 539 | 543 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 1067 | 1069 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 541 | 543 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 762 | 764 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 847 | 849 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 945 | 947 | PF00082 | 0.298 |
CLV_PCSK_PC1ET2_1 | 541 | 543 | PF00082 | 0.310 |
CLV_PCSK_PC1ET2_1 | 945 | 947 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 1009 | 1013 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 578 | 582 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 921 | 925 | PF00082 | 0.231 |
CLV_Separin_Metazoa | 781 | 785 | PF03568 | 0.492 |
DEG_APCC_DBOX_1 | 1048 | 1056 | PF00400 | 0.476 |
DEG_APCC_DBOX_1 | 1095 | 1103 | PF00400 | 0.216 |
DEG_APCC_DBOX_1 | 569 | 577 | PF00400 | 0.357 |
DOC_ANK_TNKS_1 | 588 | 595 | PF00023 | 0.415 |
DOC_CKS1_1 | 732 | 737 | PF01111 | 0.429 |
DOC_CYCLIN_yCln2_LP_2 | 199 | 205 | PF00134 | 0.559 |
DOC_CYCLIN_yCln2_LP_2 | 425 | 431 | PF00134 | 0.271 |
DOC_CYCLIN_yCln2_LP_2 | 79 | 85 | PF00134 | 0.565 |
DOC_MAPK_DCC_7 | 673 | 681 | PF00069 | 0.357 |
DOC_MAPK_FxFP_2 | 509 | 512 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 575 | 584 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 670 | 678 | PF00069 | 0.357 |
DOC_MAPK_gen_1 | 762 | 769 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 673 | 681 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 957 | 964 | PF00069 | 0.448 |
DOC_MAPK_RevD_3 | 1053 | 1068 | PF00069 | 0.478 |
DOC_PP1_RVXF_1 | 1007 | 1013 | PF00149 | 0.448 |
DOC_PP2B_LxvP_1 | 1082 | 1085 | PF13499 | 0.331 |
DOC_PP2B_LxvP_1 | 199 | 202 | PF13499 | 0.558 |
DOC_PP2B_LxvP_1 | 346 | 349 | PF13499 | 0.359 |
DOC_PP2B_LxvP_1 | 425 | 428 | PF13499 | 0.331 |
DOC_PP2B_LxvP_1 | 66 | 69 | PF13499 | 0.560 |
DOC_PP2B_LxvP_1 | 79 | 82 | PF13499 | 0.538 |
DOC_PP2B_LxvP_1 | 906 | 909 | PF13499 | 0.357 |
DOC_PP4_FxxP_1 | 509 | 512 | PF00568 | 0.391 |
DOC_USP7_MATH_1 | 1085 | 1089 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 564 | 568 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 706 | 710 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 866 | 870 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.596 |
DOC_WW_Pin1_4 | 1017 | 1022 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 731 | 736 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 791 | 796 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 868 | 873 | PF00397 | 0.470 |
LIG_14-3-3_CanoR_1 | 1059 | 1066 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 119 | 123 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 194 | 202 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 50 | 55 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 515 | 520 | PF00244 | 0.275 |
LIG_14-3-3_CanoR_1 | 539 | 549 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 57 | 62 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 570 | 574 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 670 | 676 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 784 | 790 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 84 | 94 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 921 | 927 | PF00244 | 0.389 |
LIG_APCC_ABBA_1 | 435 | 440 | PF00400 | 0.328 |
LIG_BIR_III_2 | 697 | 701 | PF00653 | 0.509 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.732 |
LIG_BRCT_BRCA1_1 | 247 | 251 | PF00533 | 0.509 |
LIG_Clathr_ClatBox_1 | 31 | 35 | PF01394 | 0.367 |
LIG_Clathr_ClatBox_1 | 392 | 396 | PF01394 | 0.506 |
LIG_CtBP_PxDLS_1 | 114 | 118 | PF00389 | 0.569 |
LIG_deltaCOP1_diTrp_1 | 707 | 717 | PF00928 | 0.490 |
LIG_EH1_1 | 482 | 490 | PF00400 | 0.475 |
LIG_eIF4E_1 | 483 | 489 | PF01652 | 0.556 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.605 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.712 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.673 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.519 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.634 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.472 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.410 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.454 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.510 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.265 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.462 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.301 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.465 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.435 |
LIG_FHA_1 | 684 | 690 | PF00498 | 0.509 |
LIG_FHA_1 | 770 | 776 | PF00498 | 0.437 |
LIG_FHA_1 | 922 | 928 | PF00498 | 0.376 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.626 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.481 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.431 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.479 |
LIG_FHA_2 | 516 | 522 | PF00498 | 0.271 |
LIG_FHA_2 | 593 | 599 | PF00498 | 0.471 |
LIG_GBD_Chelix_1 | 431 | 439 | PF00786 | 0.232 |
LIG_Integrin_isoDGR_2 | 919 | 921 | PF01839 | 0.157 |
LIG_KLC1_Yacidic_2 | 1132 | 1136 | PF13176 | 0.467 |
LIG_LIR_Apic_2 | 507 | 512 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 248 | 259 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 382 | 393 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 496 | 506 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 527 | 536 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 707 | 718 | PF02991 | 0.429 |
LIG_LIR_LC3C_4 | 324 | 329 | PF02991 | 0.487 |
LIG_LIR_LC3C_4 | 500 | 503 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.708 |
LIG_LIR_Nem_3 | 496 | 502 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 527 | 532 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 674 | 678 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 707 | 713 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.586 |
LIG_LYPXL_S_1 | 1091 | 1095 | PF13949 | 0.381 |
LIG_MAD2 | 583 | 591 | PF02301 | 0.415 |
LIG_MYND_1 | 262 | 266 | PF01753 | 0.401 |
LIG_MYND_1 | 81 | 85 | PF01753 | 0.672 |
LIG_MYND_3 | 63 | 67 | PF01753 | 0.539 |
LIG_NRBOX | 1051 | 1057 | PF00104 | 0.464 |
LIG_PCNA_PIPBox_1 | 513 | 522 | PF02747 | 0.157 |
LIG_Pex14_1 | 1075 | 1079 | PF04695 | 0.271 |
LIG_Pex14_2 | 1073 | 1077 | PF04695 | 0.271 |
LIG_Pex14_2 | 131 | 135 | PF04695 | 0.673 |
LIG_Pex14_2 | 471 | 475 | PF04695 | 0.488 |
LIG_Pex14_2 | 678 | 682 | PF04695 | 0.509 |
LIG_Pex14_2 | 713 | 717 | PF04695 | 0.417 |
LIG_PTB_Apo_2 | 893 | 900 | PF02174 | 0.357 |
LIG_REV1ctd_RIR_1 | 1092 | 1099 | PF16727 | 0.414 |
LIG_SH2_CRK | 1079 | 1083 | PF00017 | 0.296 |
LIG_SH2_CRK | 499 | 503 | PF00017 | 0.331 |
LIG_SH2_CRK | 890 | 894 | PF00017 | 0.425 |
LIG_SH2_SRC | 497 | 500 | PF00017 | 0.271 |
LIG_SH2_STAP1 | 279 | 283 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 323 | 327 | PF00017 | 0.589 |
LIG_SH2_STAP1 | 499 | 503 | PF00017 | 0.384 |
LIG_SH2_STAT3 | 56 | 59 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 1124 | 1127 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.615 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.175 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.168 |
LIG_SH2_STAT5 | 813 | 816 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 890 | 893 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 954 | 957 | PF00017 | 0.472 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.595 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.781 |
LIG_SH3_3 | 880 | 886 | PF00018 | 0.473 |
LIG_SH3_4 | 661 | 668 | PF00018 | 0.415 |
LIG_SUMO_SIM_anti_2 | 1050 | 1057 | PF11976 | 0.478 |
LIG_SUMO_SIM_anti_2 | 1111 | 1119 | PF11976 | 0.296 |
LIG_SUMO_SIM_par_1 | 1080 | 1086 | PF11976 | 0.268 |
LIG_SUMO_SIM_par_1 | 30 | 35 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 389 | 398 | PF11976 | 0.568 |
LIG_SUMO_SIM_par_1 | 486 | 493 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 936 | 943 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 961 | 966 | PF11976 | 0.429 |
LIG_TRAF2_1 | 2 | 5 | PF00917 | 0.357 |
LIG_TRAF2_1 | 619 | 622 | PF00917 | 0.452 |
LIG_WRC_WIRS_1 | 526 | 531 | PF05994 | 0.296 |
LIG_WW_3 | 885 | 889 | PF00397 | 0.470 |
MOD_CK1_1 | 1062 | 1068 | PF00069 | 0.496 |
MOD_CK1_1 | 1111 | 1117 | PF00069 | 0.279 |
MOD_CK1_1 | 1118 | 1124 | PF00069 | 0.260 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.357 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.691 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.434 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.500 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.661 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.356 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.679 |
MOD_CK1_1 | 683 | 689 | PF00069 | 0.509 |
MOD_CK1_1 | 855 | 861 | PF00069 | 0.528 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.642 |
MOD_CK1_1 | 874 | 880 | PF00069 | 0.509 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.610 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.352 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.497 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.472 |
MOD_CK2_1 | 699 | 705 | PF00069 | 0.409 |
MOD_CMANNOS | 475 | 478 | PF00535 | 0.338 |
MOD_GlcNHglycan | 1087 | 1090 | PF01048 | 0.296 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.430 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.297 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.443 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.384 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.339 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.370 |
MOD_GlcNHglycan | 753 | 756 | PF01048 | 0.300 |
MOD_GlcNHglycan | 789 | 792 | PF01048 | 0.188 |
MOD_GlcNHglycan | 830 | 833 | PF01048 | 0.334 |
MOD_GlcNHglycan | 839 | 843 | PF01048 | 0.263 |
MOD_GSK3_1 | 1111 | 1118 | PF00069 | 0.274 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.676 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.683 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.762 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.653 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.496 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.556 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.488 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.431 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.613 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.590 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.279 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.400 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.288 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.251 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.429 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.410 |
MOD_GSK3_1 | 769 | 776 | PF00069 | 0.439 |
MOD_GSK3_1 | 787 | 794 | PF00069 | 0.465 |
MOD_GSK3_1 | 851 | 858 | PF00069 | 0.454 |
MOD_GSK3_1 | 864 | 871 | PF00069 | 0.423 |
MOD_GSK3_1 | 874 | 881 | PF00069 | 0.526 |
MOD_GSK3_1 | 922 | 929 | PF00069 | 0.430 |
MOD_GSK3_1 | 977 | 984 | PF00069 | 0.438 |
MOD_N-GLC_1 | 1017 | 1022 | PF02516 | 0.247 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.270 |
MOD_N-GLC_1 | 628 | 633 | PF02516 | 0.215 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.400 |
MOD_NEK2_1 | 1108 | 1113 | PF00069 | 0.271 |
MOD_NEK2_1 | 1116 | 1121 | PF00069 | 0.271 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.682 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.646 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.509 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.472 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.440 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.494 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.480 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.498 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.269 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.421 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.331 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.534 |
MOD_NEK2_1 | 628 | 633 | PF00069 | 0.475 |
MOD_NEK2_1 | 680 | 685 | PF00069 | 0.478 |
MOD_NEK2_1 | 717 | 722 | PF00069 | 0.425 |
MOD_NEK2_1 | 739 | 744 | PF00069 | 0.432 |
MOD_NEK2_1 | 751 | 756 | PF00069 | 0.488 |
MOD_NEK2_1 | 769 | 774 | PF00069 | 0.488 |
MOD_NEK2_1 | 955 | 960 | PF00069 | 0.444 |
MOD_NEK2_2 | 504 | 509 | PF00069 | 0.333 |
MOD_NEK2_2 | 95 | 100 | PF00069 | 0.543 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.689 |
MOD_PK_1 | 57 | 63 | PF00069 | 0.495 |
MOD_PKA_1 | 541 | 547 | PF00069 | 0.464 |
MOD_PKA_2 | 1005 | 1011 | PF00069 | 0.357 |
MOD_PKA_2 | 1048 | 1054 | PF00069 | 0.486 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.745 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.707 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.700 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.357 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.464 |
MOD_PKA_2 | 569 | 575 | PF00069 | 0.509 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.663 |
MOD_PKB_1 | 408 | 416 | PF00069 | 0.469 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.710 |
MOD_Plk_1 | 184 | 190 | PF00069 | 0.700 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.470 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.525 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.519 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.671 |
MOD_Plk_1 | 642 | 648 | PF00069 | 0.455 |
MOD_Plk_1 | 706 | 712 | PF00069 | 0.512 |
MOD_Plk_1 | 851 | 857 | PF00069 | 0.528 |
MOD_Plk_1 | 864 | 870 | PF00069 | 0.499 |
MOD_Plk_1 | 878 | 884 | PF00069 | 0.509 |
MOD_Plk_2-3 | 156 | 162 | PF00069 | 0.635 |
MOD_Plk_2-3 | 598 | 604 | PF00069 | 0.429 |
MOD_Plk_4 | 1048 | 1054 | PF00069 | 0.475 |
MOD_Plk_4 | 1111 | 1117 | PF00069 | 0.331 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.715 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.505 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.289 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.419 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.252 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.280 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.159 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.263 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.495 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.473 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.402 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.442 |
MOD_Plk_4 | 642 | 648 | PF00069 | 0.410 |
MOD_Plk_4 | 718 | 724 | PF00069 | 0.469 |
MOD_Plk_4 | 852 | 858 | PF00069 | 0.543 |
MOD_Plk_4 | 922 | 928 | PF00069 | 0.473 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.542 |
MOD_ProDKin_1 | 1017 | 1023 | PF00069 | 0.457 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.561 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.650 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.514 |
MOD_ProDKin_1 | 731 | 737 | PF00069 | 0.429 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.779 |
MOD_ProDKin_1 | 791 | 797 | PF00069 | 0.421 |
MOD_ProDKin_1 | 868 | 874 | PF00069 | 0.470 |
MOD_SUMO_for_1 | 944 | 947 | PF00179 | 0.415 |
MOD_SUMO_rev_2 | 229 | 238 | PF00179 | 0.470 |
TRG_DiLeu_BaEn_1 | 160 | 165 | PF01217 | 0.731 |
TRG_DiLeu_BaEn_1 | 550 | 555 | PF01217 | 0.565 |
TRG_DiLeu_BaEn_1 | 910 | 915 | PF01217 | 0.478 |
TRG_DiLeu_BaEn_4 | 160 | 166 | PF01217 | 0.673 |
TRG_DiLeu_BaLyEn_6 | 442 | 447 | PF01217 | 0.422 |
TRG_ENDOCYTIC_2 | 1070 | 1073 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 1079 | 1082 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 1092 | 1095 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 499 | 502 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 890 | 893 | PF00928 | 0.425 |
TRG_ER_diArg_1 | 1066 | 1068 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.679 |
TRG_ER_diArg_1 | 136 | 138 | PF00400 | 0.662 |
TRG_ER_diArg_1 | 761 | 763 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 846 | 848 | PF00400 | 0.357 |
TRG_Pf-PMV_PEXEL_1 | 1001 | 1005 | PF00026 | 0.272 |
TRG_Pf-PMV_PEXEL_1 | 410 | 414 | PF00026 | 0.385 |
TRG_Pf-PMV_PEXEL_1 | 583 | 588 | PF00026 | 0.215 |
TRG_Pf-PMV_PEXEL_1 | 833 | 837 | PF00026 | 0.309 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFW0 | Leptomonas seymouri | 61% | 100% |
A0A0S4J742 | Bodo saltans | 40% | 100% |
A0A1X0P531 | Trypanosomatidae | 51% | 100% |
A0A3Q8IGY9 | Leishmania donovani | 81% | 98% |
A0A422NN19 | Trypanosoma rangeli | 49% | 100% |
A3AWA4 | Oryza sativa subsp. japonica | 34% | 100% |
A4I980 | Leishmania infantum | 81% | 98% |
A5IVY3 | Staphylococcus aureus (strain JH9) | 33% | 100% |
A6QK47 | Staphylococcus aureus (strain Newman) | 33% | 100% |
A6U4T8 | Staphylococcus aureus (strain JH1) | 33% | 100% |
A7X6S1 | Staphylococcus aureus (strain Mu3 / ATCC 700698) | 33% | 100% |
A8Z3F8 | Staphylococcus aureus (strain USA300 / TCH1516) | 33% | 100% |
B9DFX7 | Arabidopsis thaliana | 29% | 100% |
D0A5R6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9B447 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 91% |
O29777 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 34% | 100% |
O32220 | Bacillus subtilis (strain 168) | 32% | 100% |
O33533 | Rhizobium leguminosarum bv. viciae | 28% | 100% |
O59666 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
P35670 | Homo sapiens | 32% | 78% |
P37386 | Staphylococcus aureus | 26% | 100% |
P38995 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
P46839 | Mycobacterium leprae (strain TN) | 33% | 100% |
P49015 | Cricetulus griseus | 31% | 77% |
P58341 | Rhizobium meliloti (strain 1021) | 33% | 100% |
P58342 | Rhizobium meliloti (strain 1021) | 33% | 100% |
P70705 | Rattus norvegicus | 29% | 76% |
P9WPU0 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 34% | 100% |
P9WPU1 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 34% | 100% |
Q04656 | Homo sapiens | 33% | 76% |
Q2FDV0 | Staphylococcus aureus (strain USA300) | 33% | 100% |
Q2FV64 | Staphylococcus aureus (strain NCTC 8325 / PS 47) | 33% | 100% |
Q2YWA3 | Staphylococcus aureus (strain bovine RF122 / ET3-1) | 33% | 100% |
Q4A0G1 | Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM 20229 / NCIMB 8711 / NCTC 7292 / S-41) | 32% | 100% |
Q4L970 | Staphylococcus haemolyticus (strain JCSC1435) | 33% | 100% |
Q4Q3X8 | Leishmania major | 81% | 100% |
Q59385 | Escherichia coli (strain K12) | 33% | 100% |
Q5HCZ3 | Staphylococcus aureus (strain COL) | 33% | 100% |
Q5HL56 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 32% | 100% |
Q64430 | Mus musculus | 32% | 76% |
Q64446 | Mus musculus | 32% | 78% |
Q64535 | Rattus norvegicus | 30% | 78% |
Q6G6B7 | Staphylococcus aureus (strain MSSA476) | 33% | 100% |
Q6GDP1 | Staphylococcus aureus (strain MRSA252) | 33% | 100% |
Q6H7M3 | Oryza sativa subsp. japonica | 34% | 100% |
Q7A3E6 | Staphylococcus aureus (strain N315) | 33% | 100% |
Q8CN02 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 32% | 100% |
Q8NUQ9 | Staphylococcus aureus (strain MW2) | 33% | 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) | 33% | 100% |
Q9KPZ7 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 32% | 100% |
Q9S7J8 | Arabidopsis thaliana | 34% | 100% |
Q9SH30 | Arabidopsis thaliana | 34% | 100% |
Q9SZC9 | Arabidopsis thaliana | 31% | 100% |
Q9X5X3 | Sinorhizobium medicae (strain WSM419) | 32% | 100% |
Q9XT50 | Ovis aries | 34% | 75% |