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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HB36
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 6 |
GO:0008104 | protein localization | 4 | 6 |
GO:0009306 | protein secretion | 4 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0015031 | protein transport | 4 | 6 |
GO:0030254 | protein secretion by the type III secretion system | 4 | 6 |
GO:0032940 | secretion by cell | 3 | 6 |
GO:0033036 | macromolecule localization | 2 | 6 |
GO:0035592 | establishment of protein localization to extracellular region | 4 | 6 |
GO:0045184 | establishment of protein localization | 3 | 6 |
GO:0046903 | secretion | 4 | 6 |
GO:0051179 | localization | 1 | 6 |
GO:0051234 | establishment of localization | 2 | 6 |
GO:0051641 | cellular localization | 2 | 6 |
GO:0055085 | transmembrane transport | 2 | 6 |
GO:0070727 | cellular macromolecule localization | 3 | 6 |
GO:0071692 | protein localization to extracellular region | 5 | 6 |
GO:0071702 | organic substance transport | 4 | 6 |
GO:0071705 | nitrogen compound transport | 4 | 6 |
GO:0071806 | protein transmembrane transport | 3 | 6 |
GO:0140352 | export from cell | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 18 | 22 | PF00656 | 0.637 |
CLV_C14_Caspase3-7 | 427 | 431 | PF00656 | 0.387 |
CLV_C14_Caspase3-7 | 560 | 564 | PF00656 | 0.356 |
CLV_C14_Caspase3-7 | 70 | 74 | PF00656 | 0.560 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 569 | 571 | PF00675 | 0.488 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 569 | 571 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 198 | 200 | PF00082 | 0.606 |
CLV_PCSK_PC1ET2_1 | 42 | 44 | PF00082 | 0.654 |
CLV_PCSK_PC7_1 | 327 | 333 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.251 |
DEG_APCC_DBOX_1 | 372 | 380 | PF00400 | 0.553 |
DEG_APCC_DBOX_1 | 496 | 504 | PF00400 | 0.636 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.857 |
DEG_SCF_FBW7_2 | 546 | 553 | PF00400 | 0.455 |
DEG_SPOP_SBC_1 | 162 | 166 | PF00917 | 0.587 |
DEG_SPOP_SBC_1 | 9 | 13 | PF00917 | 0.430 |
DOC_CDC14_PxL_1 | 481 | 489 | PF14671 | 0.455 |
DOC_CYCLIN_RxL_1 | 315 | 329 | PF00134 | 0.648 |
DOC_MAPK_MEF2A_6 | 475 | 484 | PF00069 | 0.622 |
DOC_PP2B_LxvP_1 | 170 | 173 | PF13499 | 0.722 |
DOC_PP2B_LxvP_1 | 482 | 485 | PF13499 | 0.455 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.449 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.840 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.827 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.508 |
LIG_14-3-3_CanoR_1 | 106 | 113 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 213 | 221 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 373 | 377 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 381 | 387 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 489 | 495 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 537 | 544 | PF00244 | 0.483 |
LIG_Actin_WH2_2 | 523 | 539 | PF00022 | 0.636 |
LIG_BRCT_BRCA1_1 | 181 | 185 | PF00533 | 0.581 |
LIG_Clathr_ClatBox_1 | 470 | 474 | PF01394 | 0.636 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.621 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.615 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.431 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.594 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.411 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.545 |
LIG_FHA_1 | 557 | 563 | PF00498 | 0.658 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.370 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.664 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.638 |
LIG_FHA_2 | 336 | 342 | PF00498 | 0.674 |
LIG_FHA_2 | 558 | 564 | PF00498 | 0.347 |
LIG_LIR_Gen_1 | 478 | 487 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 59 | 65 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 478 | 484 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 59 | 63 | PF02991 | 0.678 |
LIG_SH2_CRK | 25 | 29 | PF00017 | 0.620 |
LIG_SH2_PTP2 | 483 | 486 | PF00017 | 0.636 |
LIG_SH2_STAP1 | 283 | 287 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 501 | 505 | PF00017 | 0.636 |
LIG_SH2_STAT3 | 207 | 210 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.661 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.618 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.805 |
LIG_SUMO_SIM_anti_2 | 32 | 37 | PF11976 | 0.393 |
LIG_SUMO_SIM_anti_2 | 322 | 329 | PF11976 | 0.652 |
LIG_SUMO_SIM_par_1 | 469 | 474 | PF11976 | 0.636 |
LIG_TRAF2_1 | 338 | 341 | PF00917 | 0.674 |
LIG_WRC_WIRS_1 | 57 | 62 | PF05994 | 0.653 |
MOD_CDC14_SPxK_1 | 133 | 136 | PF00782 | 0.622 |
MOD_CDK_SPK_2 | 101 | 106 | PF00069 | 0.578 |
MOD_CDK_SPK_2 | 130 | 135 | PF00069 | 0.840 |
MOD_CDK_SPK_2 | 163 | 168 | PF00069 | 0.735 |
MOD_CDK_SPxK_1 | 130 | 136 | PF00069 | 0.626 |
MOD_CDK_SPxxK_3 | 408 | 415 | PF00069 | 0.562 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.583 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.817 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.756 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.601 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.560 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.638 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.482 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.418 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.690 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.809 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.673 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.667 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.556 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.521 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.765 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.793 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.567 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.650 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.553 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.338 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.427 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.373 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.650 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.790 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.699 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.739 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.630 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.714 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.584 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.598 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.562 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.637 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.511 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.642 |
MOD_N-GLC_1 | 179 | 184 | PF02516 | 0.579 |
MOD_N-GLC_1 | 455 | 460 | PF02516 | 0.435 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.404 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.407 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.575 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.521 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.439 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.492 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.657 |
MOD_NEK2_2 | 10 | 15 | PF00069 | 0.400 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.594 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.674 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.556 |
MOD_PIKK_1 | 336 | 342 | PF00454 | 0.421 |
MOD_PKA_1 | 198 | 204 | PF00069 | 0.559 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.538 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.738 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.559 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.506 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.667 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.586 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.636 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.636 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.573 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.636 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.613 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.391 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.543 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.770 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.840 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.826 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.615 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.559 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.456 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.518 |
MOD_SUMO_for_1 | 314 | 317 | PF00179 | 0.645 |
MOD_SUMO_for_1 | 358 | 361 | PF00179 | 0.585 |
MOD_SUMO_rev_2 | 248 | 254 | PF00179 | 0.473 |
MOD_SUMO_rev_2 | 280 | 290 | PF00179 | 0.609 |
MOD_SUMO_rev_2 | 335 | 344 | PF00179 | 0.677 |
TRG_DiLeu_BaEn_4 | 285 | 291 | PF01217 | 0.651 |
TRG_DiLeu_BaLyEn_6 | 482 | 487 | PF01217 | 0.455 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.620 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.618 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.521 |
TRG_ER_diArg_1 | 261 | 264 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 330 | 332 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 569 | 571 | PF00400 | 0.488 |
TRG_NES_CRM1_1 | 247 | 259 | PF08389 | 0.638 |
TRG_NES_CRM1_1 | 55 | 67 | PF08389 | 0.655 |
TRG_NLS_MonoExtC_3 | 38 | 43 | PF00514 | 0.635 |
TRG_Pf-PMV_PEXEL_1 | 356 | 361 | PF00026 | 0.664 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IIE0 | Leishmania donovani | 72% | 100% |
A4IAN3 | Leishmania infantum | 72% | 100% |
E9B5A6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4Q2M7 | Leishmania major | 69% | 100% |