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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A0A3S7WPX2
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0016491 | oxidoreductase activity | 2 | 8 |
GO:0020037 | heme binding | 4 | 6 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
GO:0046906 | tetrapyrrole binding | 3 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0010181 | FMN binding | 4 | 2 |
GO:0032553 | ribonucleotide binding | 3 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0097367 | carbohydrate derivative binding | 2 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 476 | 480 | PF00656 | 0.333 |
CLV_C14_Caspase3-7 | 585 | 589 | PF00656 | 0.484 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.314 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 595 | 597 | PF00082 | 0.413 |
CLV_PCSK_PC1ET2_1 | 355 | 357 | PF00082 | 0.338 |
CLV_PCSK_PC1ET2_1 | 403 | 405 | PF00082 | 0.275 |
CLV_PCSK_PC1ET2_1 | 416 | 418 | PF00082 | 0.202 |
CLV_PCSK_PC1ET2_1 | 595 | 597 | PF00082 | 0.413 |
CLV_PCSK_PC7_1 | 351 | 357 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.234 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 592 | 596 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.254 |
DEG_ODPH_VHL_1 | 458 | 471 | PF01847 | 0.292 |
DOC_CYCLIN_RxL_1 | 523 | 531 | PF00134 | 0.401 |
DOC_CYCLIN_RxL_1 | 613 | 624 | PF00134 | 0.292 |
DOC_MAPK_gen_1 | 142 | 150 | PF00069 | 0.333 |
DOC_PP1_RVXF_1 | 124 | 130 | PF00149 | 0.292 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.255 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.267 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.638 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.224 |
DOC_WW_Pin1_4 | 658 | 663 | PF00397 | 0.333 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.310 |
LIG_14-3-3_CanoR_1 | 404 | 413 | PF00244 | 0.292 |
LIG_APCC_ABBA_1 | 75 | 80 | PF00400 | 0.254 |
LIG_BIR_III_2 | 580 | 584 | PF00653 | 0.579 |
LIG_BRCT_BRCA1_1 | 407 | 411 | PF00533 | 0.229 |
LIG_Clathr_ClatBox_1 | 260 | 264 | PF01394 | 0.333 |
LIG_deltaCOP1_diTrp_1 | 114 | 120 | PF00928 | 0.273 |
LIG_eIF4E_1 | 348 | 354 | PF01652 | 0.302 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.306 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.314 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.204 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.386 |
LIG_FHA_1 | 621 | 627 | PF00498 | 0.333 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.273 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.610 |
LIG_FHA_2 | 596 | 602 | PF00498 | 0.241 |
LIG_GBD_Chelix_1 | 614 | 622 | PF00786 | 0.292 |
LIG_LIR_Apic_2 | 531 | 535 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 151 | 160 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 327 | 338 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 543 | 553 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 609 | 620 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 645 | 656 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 151 | 155 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 377 | 381 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 543 | 548 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 609 | 615 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 645 | 651 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 85 | 89 | PF02991 | 0.310 |
LIG_MAD2 | 176 | 184 | PF02301 | 0.347 |
LIG_PCNA_yPIPBox_3 | 502 | 515 | PF02747 | 0.246 |
LIG_Pex14_1 | 115 | 119 | PF04695 | 0.292 |
LIG_Pex14_2 | 215 | 219 | PF04695 | 0.333 |
LIG_Pex14_2 | 407 | 411 | PF04695 | 0.204 |
LIG_SH2_CRK | 152 | 156 | PF00017 | 0.292 |
LIG_SH2_CRK | 516 | 520 | PF00017 | 0.316 |
LIG_SH2_CRK | 532 | 536 | PF00017 | 0.457 |
LIG_SH2_GRB2like | 119 | 122 | PF00017 | 0.267 |
LIG_SH2_NCK_1 | 152 | 156 | PF00017 | 0.292 |
LIG_SH2_NCK_1 | 597 | 601 | PF00017 | 0.292 |
LIG_SH2_STAP1 | 545 | 549 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.220 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 597 | 600 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 660 | 663 | PF00017 | 0.333 |
LIG_SH3_1 | 94 | 100 | PF00018 | 0.254 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.368 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.273 |
LIG_SH3_3 | 551 | 557 | PF00018 | 0.524 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.537 |
LIG_SH3_3 | 624 | 630 | PF00018 | 0.333 |
LIG_SH3_3 | 648 | 654 | PF00018 | 0.292 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.254 |
LIG_SUMO_SIM_anti_2 | 37 | 42 | PF11976 | 0.251 |
LIG_SUMO_SIM_par_1 | 37 | 42 | PF11976 | 0.251 |
LIG_TYR_ITIM | 150 | 155 | PF00017 | 0.292 |
LIG_TYR_ITIM | 514 | 519 | PF00017 | 0.318 |
LIG_UBA3_1 | 154 | 163 | PF00899 | 0.273 |
LIG_UBA3_1 | 410 | 416 | PF00899 | 0.204 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.244 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.435 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.688 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.229 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.456 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.292 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.254 |
MOD_CK2_1 | 595 | 601 | PF00069 | 0.295 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.279 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.328 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.317 |
MOD_GlcNHglycan | 335 | 339 | PF01048 | 0.365 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.329 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.292 |
MOD_GlcNHglycan | 42 | 46 | PF01048 | 0.275 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.221 |
MOD_GlcNHglycan | 574 | 578 | PF01048 | 0.512 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.241 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.296 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.337 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.261 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.428 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.222 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.579 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.293 |
MOD_LATS_1 | 133 | 139 | PF00433 | 0.333 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.261 |
MOD_N-GLC_1 | 620 | 625 | PF02516 | 0.292 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.257 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.273 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.325 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.330 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.392 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.424 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.292 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.389 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.548 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.251 |
MOD_PKA_1 | 595 | 601 | PF00069 | 0.273 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.273 |
MOD_PKA_2 | 595 | 601 | PF00069 | 0.292 |
MOD_PKB_1 | 168 | 176 | PF00069 | 0.267 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.287 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.227 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.251 |
MOD_Plk_2-3 | 445 | 451 | PF00069 | 0.292 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.251 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.213 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.236 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.229 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.333 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.240 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.405 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.479 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.333 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.337 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.401 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.734 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.224 |
MOD_ProDKin_1 | 658 | 664 | PF00069 | 0.333 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.310 |
MOD_SUMO_for_1 | 369 | 372 | PF00179 | 0.245 |
MOD_SUMO_rev_2 | 473 | 482 | PF00179 | 0.292 |
MOD_SUMO_rev_2 | 567 | 575 | PF00179 | 0.511 |
MOD_SUMO_rev_2 | 588 | 594 | PF00179 | 0.456 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 516 | 519 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 545 | 548 | PF00928 | 0.462 |
TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.267 |
TRG_NES_CRM1_1 | 66 | 81 | PF08389 | 0.254 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5C0 | Leptomonas seymouri | 37% | 100% |
A0A0S4IHN0 | Bodo saltans | 39% | 100% |
A0A0S4KND3 | Bodo saltans | 53% | 100% |
A0A1X0NPF8 | Trypanosomatidae | 57% | 99% |
A0A3S7X915 | Leishmania donovani | 36% | 100% |
A0A422MX37 | Trypanosoma rangeli | 34% | 100% |
A4HME0 | Leishmania braziliensis | 36% | 94% |
A4HME1 | Leishmania braziliensis | 35% | 100% |
A4HTA6 | Leishmania infantum | 100% | 100% |
A4IB13 | Leishmania infantum | 35% | 92% |
B2GCE0 | Limosilactobacillus fermentum (strain NBRC 3956 / LMG 18251) | 27% | 100% |
B5XRB0 | Klebsiella pneumoniae (strain 342) | 30% | 73% |
C8WLE3 | Eggerthella lenta (strain ATCC 25559 / DSM 2243 / CCUG 17323 / JCM 9979 / KCTC 3265 / NCTC 11813 / VPI 0255 / 1899 B) | 27% | 100% |
C9ZQ34 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 74% |
E9AEU2 | Leishmania major | 36% | 92% |
E9AL95 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9B5Z8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 92% |
O13755 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 100% |
P0C278 | Shewanella frigidimarina | 33% | 100% |
P21375 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 100% |
P32614 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 100% |
P83223 | Shewanella oneidensis (strain MR-1) | 34% | 100% |
Q07WU7 | Shewanella frigidimarina (strain NCIMB 400) | 33% | 100% |
Q4QIK9 | Leishmania major | 95% | 100% |
Q8CVD0 | Shewanella oneidensis (strain MR-1) | 30% | 100% |
Q9Z4P0 | Shewanella frigidimarina (strain NCIMB 400) | 31% | 100% |