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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A0A3Q8IHF7
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016757 | glycosyltransferase activity | 3 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 301 | 305 | PF00656 | 0.465 |
CLV_MEL_PAP_1 | 585 | 591 | PF00089 | 0.575 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.792 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.528 |
CLV_PCSK_FUR_1 | 629 | 633 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.747 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.792 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.725 |
CLV_PCSK_PC1ET2_1 | 115 | 117 | PF00082 | 0.692 |
CLV_PCSK_PC1ET2_1 | 631 | 633 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 8 | 10 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.618 |
DEG_APCC_DBOX_1 | 414 | 422 | PF00400 | 0.307 |
DOC_CYCLIN_RxL_1 | 474 | 484 | PF00134 | 0.284 |
DOC_MAPK_FxFP_2 | 613 | 616 | PF00069 | 0.430 |
DOC_MAPK_gen_1 | 259 | 267 | PF00069 | 0.396 |
DOC_MAPK_gen_1 | 48 | 58 | PF00069 | 0.512 |
DOC_MAPK_gen_1 | 548 | 555 | PF00069 | 0.396 |
DOC_MAPK_JIP1_4 | 475 | 481 | PF00069 | 0.249 |
DOC_MAPK_MEF2A_6 | 266 | 275 | PF00069 | 0.431 |
DOC_MAPK_MEF2A_6 | 523 | 531 | PF00069 | 0.332 |
DOC_PP2B_LxvP_1 | 308 | 311 | PF13499 | 0.526 |
DOC_PP4_FxxP_1 | 102 | 105 | PF00568 | 0.465 |
DOC_PP4_FxxP_1 | 196 | 199 | PF00568 | 0.466 |
DOC_PP4_FxxP_1 | 345 | 348 | PF00568 | 0.389 |
DOC_PP4_FxxP_1 | 613 | 616 | PF00568 | 0.430 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.794 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.359 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.306 |
DOC_WW_Pin1_4 | 542 | 547 | PF00397 | 0.386 |
LIG_14-3-3_CanoR_1 | 103 | 112 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 181 | 186 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 223 | 231 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 39 | 47 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 48 | 54 | PF00244 | 0.601 |
LIG_Actin_WH2_2 | 280 | 298 | PF00022 | 0.372 |
LIG_APCC_ABBA_1 | 622 | 627 | PF00400 | 0.348 |
LIG_BRCT_BRCA1_1 | 358 | 362 | PF00533 | 0.444 |
LIG_deltaCOP1_diTrp_1 | 423 | 429 | PF00928 | 0.332 |
LIG_eIF4E_1 | 356 | 362 | PF01652 | 0.488 |
LIG_eIF4E_1 | 474 | 480 | PF01652 | 0.267 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.477 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.396 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.435 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.450 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.472 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.315 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.465 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.386 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.455 |
LIG_Integrin_RGD_1 | 328 | 330 | PF01839 | 0.636 |
LIG_KLC1_Yacidic_2 | 506 | 511 | PF13176 | 0.307 |
LIG_LIR_Apic_2 | 194 | 199 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 123 | 133 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 282 | 292 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 282 | 288 | PF02991 | 0.449 |
LIG_MYND_3 | 410 | 414 | PF01753 | 0.271 |
LIG_PTB_Apo_2 | 204 | 211 | PF02174 | 0.452 |
LIG_PTB_Phospho_1 | 204 | 210 | PF10480 | 0.454 |
LIG_SH2_CRK | 577 | 581 | PF00017 | 0.376 |
LIG_SH2_SRC | 524 | 527 | PF00017 | 0.292 |
LIG_SH2_STAP1 | 524 | 528 | PF00017 | 0.292 |
LIG_SH2_STAT3 | 419 | 422 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.337 |
LIG_SH3_2 | 383 | 388 | PF14604 | 0.480 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.684 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.527 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.582 |
LIG_SH3_3 | 561 | 567 | PF00018 | 0.452 |
LIG_SH3_3 | 577 | 583 | PF00018 | 0.421 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.359 |
LIG_SUMO_SIM_anti_2 | 242 | 247 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 567 | 572 | PF11976 | 0.391 |
LIG_TRAF2_1 | 439 | 442 | PF00917 | 0.343 |
LIG_TRAF2_1 | 596 | 599 | PF00917 | 0.436 |
LIG_WRC_WIRS_1 | 615 | 620 | PF05994 | 0.405 |
LIG_WRPW_2 | 555 | 558 | PF00400 | 0.374 |
LIG_WW_3 | 384 | 388 | PF00397 | 0.507 |
LIG_WW_3 | 545 | 549 | PF00397 | 0.383 |
MOD_CDC14_SPxK_1 | 545 | 548 | PF00782 | 0.414 |
MOD_CDK_SPK_2 | 198 | 203 | PF00069 | 0.488 |
MOD_CDK_SPxK_1 | 542 | 548 | PF00069 | 0.391 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.490 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.413 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.510 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.488 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.311 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.286 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.370 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.449 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.446 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.288 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.672 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.646 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.685 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.690 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.631 |
MOD_GlcNHglycan | 336 | 340 | PF01048 | 0.672 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.409 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.612 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.577 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.462 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.415 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.489 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.444 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.482 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.354 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.294 |
MOD_N-GLC_1 | 191 | 196 | PF02516 | 0.671 |
MOD_N-GLC_1 | 206 | 211 | PF02516 | 0.718 |
MOD_N-GLC_1 | 356 | 361 | PF02516 | 0.665 |
MOD_N-GLC_1 | 374 | 379 | PF02516 | 0.566 |
MOD_N-GLC_1 | 436 | 441 | PF02516 | 0.537 |
MOD_N-GLC_1 | 489 | 494 | PF02516 | 0.563 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.581 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.476 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.528 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.721 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.432 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.322 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.494 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.602 |
MOD_NEK2_2 | 32 | 37 | PF00069 | 0.625 |
MOD_PIKK_1 | 127 | 133 | PF00454 | 0.446 |
MOD_PIKK_1 | 136 | 142 | PF00454 | 0.465 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.391 |
MOD_PIKK_1 | 361 | 367 | PF00454 | 0.412 |
MOD_PIKK_1 | 387 | 393 | PF00454 | 0.426 |
MOD_PIKK_1 | 465 | 471 | PF00454 | 0.319 |
MOD_PIKK_1 | 562 | 568 | PF00454 | 0.418 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.579 |
MOD_PKA_1 | 387 | 393 | PF00069 | 0.426 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.404 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.529 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.585 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.325 |
MOD_PKB_1 | 37 | 45 | PF00069 | 0.686 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.498 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.518 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.400 |
MOD_Plk_1 | 356 | 362 | PF00069 | 0.499 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.368 |
MOD_Plk_1 | 436 | 442 | PF00069 | 0.307 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.363 |
MOD_Plk_2-3 | 147 | 153 | PF00069 | 0.394 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.384 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.446 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.451 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.506 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.341 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.737 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.485 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.700 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.397 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.476 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.497 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.602 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.306 |
MOD_ProDKin_1 | 542 | 548 | PF00069 | 0.391 |
TRG_DiLeu_BaEn_1 | 598 | 603 | PF01217 | 0.416 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 577 | 580 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 615 | 618 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.689 |
TRG_ER_diArg_1 | 386 | 388 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 445 | 448 | PF00400 | 0.287 |
TRG_ER_diArg_1 | 547 | 550 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.510 |
TRG_NLS_MonoExtC_3 | 6 | 12 | PF00514 | 0.725 |
TRG_Pf-PMV_PEXEL_1 | 632 | 636 | PF00026 | 0.593 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBV1 | Leptomonas seymouri | 27% | 100% |
A0A0N1PD55 | Leptomonas seymouri | 47% | 100% |
A0A1X0NW39 | Trypanosomatidae | 23% | 100% |
A4H6H9 | Leishmania braziliensis | 79% | 100% |
A4HUW3 | Leishmania infantum | 99% | 100% |
E9ANK0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QH26 | Leishmania major | 93% | 100% |
V5BJI5 | Trypanosoma cruzi | 23% | 100% |