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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q2G8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 300 | 304 | PF00656 | 0.600 |
CLV_C14_Caspase3-7 | 424 | 428 | PF00656 | 0.718 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.783 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.712 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.682 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.616 |
CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 162 | 164 | PF00082 | 0.350 |
CLV_PCSK_PC1ET2_1 | 365 | 367 | PF00082 | 0.728 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.752 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.796 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.638 |
DEG_SPOP_SBC_1 | 10 | 14 | PF00917 | 0.593 |
DEG_SPOP_SBC_1 | 312 | 316 | PF00917 | 0.755 |
DEG_SPOP_SBC_1 | 80 | 84 | PF00917 | 0.800 |
DEG_SPOP_SBC_1 | 93 | 97 | PF00917 | 0.582 |
DOC_CKS1_1 | 25 | 30 | PF01111 | 0.763 |
DOC_CYCLIN_yCln2_LP_2 | 413 | 419 | PF00134 | 0.742 |
DOC_MAPK_JIP1_4 | 326 | 332 | PF00069 | 0.708 |
DOC_PP2B_LxvP_1 | 252 | 255 | PF13499 | 0.462 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.652 |
DOC_USP7_UBL2_3 | 400 | 404 | PF12436 | 0.706 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.803 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 358 | 363 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.511 |
LIG_14-3-3_CanoR_1 | 102 | 106 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 191 | 196 | PF00244 | 0.761 |
LIG_14-3-3_CanoR_1 | 406 | 414 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 497 | 503 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 67 | 76 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 79 | 88 | PF00244 | 0.776 |
LIG_BIR_III_4 | 425 | 429 | PF00653 | 0.553 |
LIG_BRCT_BRCA1_1 | 174 | 178 | PF00533 | 0.494 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.699 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.566 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.691 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.369 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.697 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.810 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.696 |
LIG_FHA_2 | 451 | 457 | PF00498 | 0.636 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.577 |
LIG_FHA_2 | 491 | 497 | PF00498 | 0.595 |
LIG_LIR_Nem_3 | 142 | 148 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 316 | 322 | PF02991 | 0.577 |
LIG_SH2_CRK | 145 | 149 | PF00017 | 0.483 |
LIG_SH2_CRK | 319 | 323 | PF00017 | 0.573 |
LIG_SH2_SRC | 145 | 148 | PF00017 | 0.573 |
LIG_SH2_STAP1 | 445 | 449 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.728 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.468 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.762 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.724 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.594 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.463 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.706 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.571 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.571 |
LIG_TRAF2_1 | 419 | 422 | PF00917 | 0.758 |
LIG_TRAF2_1 | 453 | 456 | PF00917 | 0.545 |
LIG_TRAF2_2 | 419 | 424 | PF00917 | 0.636 |
MOD_CDK_SPK_2 | 294 | 299 | PF00069 | 0.574 |
MOD_CDK_SPK_2 | 313 | 318 | PF00069 | 0.729 |
MOD_CDK_SPK_2 | 447 | 452 | PF00069 | 0.595 |
MOD_CDK_SPxK_1 | 24 | 30 | PF00069 | 0.609 |
MOD_CDK_SPxK_1 | 358 | 364 | PF00069 | 0.653 |
MOD_CDK_SPxxK_3 | 24 | 31 | PF00069 | 0.766 |
MOD_CDK_SPxxK_3 | 313 | 320 | PF00069 | 0.733 |
MOD_CDK_SPxxK_3 | 358 | 365 | PF00069 | 0.588 |
MOD_CDK_SPxxK_3 | 509 | 516 | PF00069 | 0.480 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.717 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.645 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.696 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.676 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.620 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.723 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.737 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.689 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.615 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.534 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.578 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.527 |
MOD_DYRK1A_RPxSP_1 | 24 | 28 | PF00069 | 0.765 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.713 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.717 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.709 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.688 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.376 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.656 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.733 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.700 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.691 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.681 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.564 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.741 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.640 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.758 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.662 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.755 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.636 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.719 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.737 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.592 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.673 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.451 |
MOD_N-GLC_1 | 358 | 363 | PF02516 | 0.586 |
MOD_N-GLC_1 | 385 | 390 | PF02516 | 0.797 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.693 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.532 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.444 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.421 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.724 |
MOD_NEK2_2 | 71 | 76 | PF00069 | 0.581 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.723 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.731 |
MOD_PKA_1 | 406 | 412 | PF00069 | 0.618 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.625 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.728 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.705 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.619 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.568 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.550 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.516 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.704 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.635 |
MOD_Plk_2-3 | 245 | 251 | PF00069 | 0.614 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.629 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.581 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.506 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.804 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.719 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.692 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.768 |
MOD_ProDKin_1 | 358 | 364 | PF00069 | 0.759 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.716 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.602 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.640 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.518 |
MOD_SUMO_for_1 | 419 | 422 | PF00179 | 0.758 |
MOD_SUMO_rev_2 | 206 | 210 | PF00179 | 0.688 |
TRG_DiLeu_BaEn_4 | 115 | 121 | PF01217 | 0.801 |
TRG_DiLeu_LyEn_5 | 129 | 134 | PF01217 | 0.580 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.580 |
TRG_ER_diArg_1 | 334 | 336 | PF00400 | 0.670 |
TRG_ER_diArg_1 | 405 | 407 | PF00400 | 0.733 |
TRG_NLS_MonoCore_2 | 363 | 368 | PF00514 | 0.831 |
TRG_NLS_MonoExtC_3 | 363 | 368 | PF00514 | 0.831 |
TRG_NLS_MonoExtC_3 | 402 | 407 | PF00514 | 0.723 |
TRG_NLS_MonoExtN_4 | 362 | 369 | PF00514 | 0.724 |
TRG_NLS_MonoExtN_4 | 400 | 407 | PF00514 | 0.716 |
TRG_Pf-PMV_PEXEL_1 | 432 | 436 | PF00026 | 0.694 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5K2 | Leptomonas seymouri | 38% | 89% |
A0A3Q8INS4 | Leishmania donovani | 83% | 100% |
A4HB95 | Leishmania braziliensis | 60% | 90% |
A4IAE3 | Leishmania infantum | 84% | 100% |
E9B5G7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 96% |