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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A0A3Q8IHF3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006396 | RNA processing | 6 | 8 |
GO:0006399 | tRNA metabolic process | 7 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008033 | tRNA processing | 8 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016070 | RNA metabolic process | 5 | 8 |
GO:0034470 | ncRNA processing | 7 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0034660 | ncRNA metabolic process | 6 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0016432 | tRNA-uridine aminocarboxypropyltransferase activity | 4 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 8 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 8 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 8 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.585 |
CLV_C14_Caspase3-7 | 456 | 460 | PF00656 | 0.399 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.538 |
CLV_PCSK_FUR_1 | 576 | 580 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 374 | 376 | PF00082 | 0.251 |
CLV_PCSK_PC1ET2_1 | 420 | 422 | PF00082 | 0.369 |
CLV_PCSK_PC1ET2_1 | 462 | 464 | PF00082 | 0.281 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.576 |
CLV_PCSK_PC7_1 | 492 | 498 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.497 |
CLV_Separin_Metazoa | 224 | 228 | PF03568 | 0.309 |
CLV_Separin_Metazoa | 97 | 101 | PF03568 | 0.516 |
DEG_APCC_DBOX_1 | 31 | 39 | PF00400 | 0.417 |
DEG_APCC_DBOX_1 | 518 | 526 | PF00400 | 0.551 |
DEG_SPOP_SBC_1 | 450 | 454 | PF00917 | 0.251 |
DOC_ANK_TNKS_1 | 311 | 318 | PF00023 | 0.319 |
DOC_CKS1_1 | 46 | 51 | PF01111 | 0.481 |
DOC_CYCLIN_yCln2_LP_2 | 239 | 245 | PF00134 | 0.369 |
DOC_MAPK_DCC_7 | 132 | 141 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 158 | 166 | PF00069 | 0.415 |
DOC_MAPK_gen_1 | 168 | 174 | PF00069 | 0.317 |
DOC_MAPK_gen_1 | 31 | 37 | PF00069 | 0.415 |
DOC_MAPK_gen_1 | 374 | 382 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 83 | 89 | PF00069 | 0.623 |
DOC_MAPK_MEF2A_6 | 132 | 141 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 374 | 381 | PF00069 | 0.251 |
DOC_MAPK_MEF2A_6 | 398 | 407 | PF00069 | 0.331 |
DOC_PP2B_LxvP_1 | 239 | 242 | PF13499 | 0.369 |
DOC_PP2B_LxvP_1 | 520 | 523 | PF13499 | 0.567 |
DOC_PP4_FxxP_1 | 574 | 577 | PF00568 | 0.594 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.505 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.476 |
LIG_14-3-3_CanoR_1 | 161 | 167 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 168 | 173 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 202 | 206 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 24 | 30 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 402 | 406 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 50 | 54 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 540 | 546 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 548 | 558 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 56 | 64 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 92 | 102 | PF00244 | 0.493 |
LIG_Actin_WH2_2 | 458 | 474 | PF00022 | 0.369 |
LIG_APCC_ABBA_1 | 218 | 223 | PF00400 | 0.309 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.507 |
LIG_Clathr_ClatBox_1 | 379 | 383 | PF01394 | 0.369 |
LIG_deltaCOP1_diTrp_1 | 148 | 152 | PF00928 | 0.362 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.464 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.309 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.300 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.399 |
LIG_FHA_1 | 540 | 546 | PF00498 | 0.484 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.611 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.346 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.437 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.460 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.527 |
LIG_FHA_2 | 550 | 556 | PF00498 | 0.550 |
LIG_HP1_1 | 401 | 405 | PF01393 | 0.369 |
LIG_IBAR_NPY_1 | 28 | 30 | PF08397 | 0.475 |
LIG_LIR_Apic_2 | 573 | 577 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 138 | 147 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 409 | 418 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 409 | 414 | PF02991 | 0.361 |
LIG_PTB_Apo_2 | 472 | 479 | PF02174 | 0.430 |
LIG_PTB_Apo_2 | 524 | 531 | PF02174 | 0.479 |
LIG_PTB_Phospho_1 | 524 | 530 | PF10480 | 0.488 |
LIG_SH2_CRK | 46 | 50 | PF00017 | 0.480 |
LIG_SH2_CRK | 528 | 532 | PF00017 | 0.411 |
LIG_SH2_GRB2like | 473 | 476 | PF00017 | 0.434 |
LIG_SH2_NCK_1 | 473 | 477 | PF00017 | 0.435 |
LIG_SH2_SRC | 473 | 476 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 411 | 415 | PF00017 | 0.398 |
LIG_SH2_STAP1 | 446 | 450 | PF00017 | 0.369 |
LIG_SH2_STAT3 | 254 | 257 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.375 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.452 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.284 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.627 |
LIG_SH3_3 | 585 | 591 | PF00018 | 0.625 |
LIG_SUMO_SIM_par_1 | 364 | 369 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 378 | 385 | PF11976 | 0.345 |
LIG_TRAF2_1 | 142 | 145 | PF00917 | 0.490 |
LIG_TRAF2_1 | 319 | 322 | PF00917 | 0.345 |
LIG_TRAF2_1 | 57 | 60 | PF00917 | 0.589 |
LIG_TYR_ITIM | 526 | 531 | PF00017 | 0.435 |
LIG_UBA3_1 | 414 | 420 | PF00899 | 0.309 |
LIG_WW_3 | 53 | 57 | PF00397 | 0.490 |
MOD_CDK_SPK_2 | 45 | 50 | PF00069 | 0.473 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.605 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.720 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.491 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.387 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.644 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.421 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.689 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.471 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.297 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.298 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.289 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.394 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.533 |
MOD_CK2_1 | 549 | 555 | PF00069 | 0.550 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.594 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.570 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.644 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.369 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.456 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.511 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.687 |
MOD_GlcNHglycan | 514 | 518 | PF01048 | 0.594 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.472 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.627 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.636 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.478 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.544 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.438 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.462 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.206 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.359 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.345 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.495 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.584 |
MOD_N-GLC_1 | 122 | 127 | PF02516 | 0.498 |
MOD_N-GLC_1 | 350 | 355 | PF02516 | 0.305 |
MOD_N-GLC_2 | 527 | 529 | PF02516 | 0.446 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.746 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.511 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.339 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.376 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.353 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.534 |
MOD_NEK2_2 | 277 | 282 | PF00069 | 0.369 |
MOD_PIKK_1 | 451 | 457 | PF00454 | 0.318 |
MOD_PIKK_1 | 605 | 611 | PF00454 | 0.687 |
MOD_PK_1 | 168 | 174 | PF00069 | 0.433 |
MOD_PK_1 | 83 | 89 | PF00069 | 0.409 |
MOD_PKA_1 | 168 | 174 | PF00069 | 0.402 |
MOD_PKA_1 | 419 | 425 | PF00069 | 0.309 |
MOD_PKA_1 | 83 | 89 | PF00069 | 0.515 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.402 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.406 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.322 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.557 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.399 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.287 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.660 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.398 |
MOD_PKA_2 | 591 | 597 | PF00069 | 0.646 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.409 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.583 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.537 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.398 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.346 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.369 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.309 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.428 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.537 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.447 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.309 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.346 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.368 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.369 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.399 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.491 |
MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.479 |
MOD_SUMO_for_1 | 596 | 599 | PF00179 | 0.613 |
MOD_SUMO_rev_2 | 142 | 152 | PF00179 | 0.435 |
TRG_DiLeu_BaEn_1 | 215 | 220 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_2 | 147 | 153 | PF01217 | 0.424 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.426 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.412 |
TRG_ER_diArg_1 | 167 | 169 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 418 | 421 | PF00400 | 0.369 |
TRG_ER_diArg_1 | 496 | 498 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 518 | 521 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 567 | 569 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 576 | 579 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.522 |
TRG_NLS_MonoExtC_3 | 418 | 423 | PF00514 | 0.369 |
TRG_NLS_MonoExtN_4 | 88 | 95 | PF00514 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 578 | 582 | PF00026 | 0.641 |
TRG_Pf-PMV_PEXEL_1 | 92 | 97 | PF00026 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6V5 | Leptomonas seymouri | 56% | 100% |
A0A0S4JPN0 | Bodo saltans | 37% | 100% |
A4HHL7 | Leishmania braziliensis | 75% | 100% |
A4I4S6 | Leishmania infantum | 100% | 100% |
E9AE79 | Leishmania major | 91% | 100% |
E9ALK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |