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: A0A3S7X7L7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 389 | 393 | PF00656 | 0.585 |
CLV_C14_Caspase3-7 | 484 | 488 | PF00656 | 0.650 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.836 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.593 |
CLV_PCSK_FUR_1 | 400 | 404 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.836 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.787 |
DOC_ANK_TNKS_1 | 298 | 305 | PF00023 | 0.660 |
DOC_CKS1_1 | 478 | 483 | PF01111 | 0.742 |
DOC_CYCLIN_yCln2_LP_2 | 188 | 194 | PF00134 | 0.671 |
DOC_MAPK_FxFP_2 | 111 | 114 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 436 | 444 | PF00069 | 0.692 |
DOC_MAPK_JIP1_4 | 77 | 83 | PF00069 | 0.563 |
DOC_PP1_RVXF_1 | 114 | 120 | PF00149 | 0.473 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.705 |
DOC_PP4_FxxP_1 | 111 | 114 | PF00568 | 0.508 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.812 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.662 |
DOC_USP7_UBL2_3 | 545 | 549 | PF12436 | 0.655 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.789 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.744 |
LIG_14-3-3_CanoR_1 | 154 | 159 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 297 | 302 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 351 | 359 | PF00244 | 0.747 |
LIG_Actin_WH2_2 | 531 | 547 | PF00022 | 0.761 |
LIG_BIR_III_4 | 236 | 240 | PF00653 | 0.747 |
LIG_BIR_III_4 | 487 | 491 | PF00653 | 0.553 |
LIG_deltaCOP1_diTrp_1 | 392 | 398 | PF00928 | 0.524 |
LIG_deltaCOP1_diTrp_1 | 410 | 414 | PF00928 | 0.460 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.518 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.606 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.819 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.699 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.826 |
LIG_FHA_2 | 507 | 513 | PF00498 | 0.760 |
LIG_LIR_Apic_2 | 108 | 114 | PF02991 | 0.486 |
LIG_LIR_Apic_2 | 25 | 31 | PF02991 | 0.783 |
LIG_LIR_Apic_2 | 33 | 39 | PF02991 | 0.570 |
LIG_LIR_Apic_2 | 368 | 373 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 171 | 175 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 420 | 426 | PF02991 | 0.531 |
LIG_PCNA_yPIPBox_3 | 416 | 430 | PF02747 | 0.577 |
LIG_SH2_CRK | 28 | 32 | PF00017 | 0.698 |
LIG_SH2_CRK | 36 | 40 | PF00017 | 0.695 |
LIG_SH2_NCK_1 | 36 | 40 | PF00017 | 0.788 |
LIG_SH2_NCK_1 | 370 | 374 | PF00017 | 0.642 |
LIG_SH2_SRC | 426 | 429 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.680 |
LIG_SH3_1 | 432 | 438 | PF00018 | 0.602 |
LIG_SH3_2 | 435 | 440 | PF14604 | 0.651 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.798 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.596 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.630 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.557 |
LIG_SH3_3 | 525 | 531 | PF00018 | 0.700 |
LIG_UBA3_1 | 169 | 176 | PF00899 | 0.574 |
LIG_UBA3_1 | 537 | 545 | PF00899 | 0.633 |
LIG_WRC_WIRS_1 | 86 | 91 | PF05994 | 0.516 |
LIG_WW_3 | 378 | 382 | PF00397 | 0.697 |
MOD_CDK_SPxK_1 | 156 | 162 | PF00069 | 0.625 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.564 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.685 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.594 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.784 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.805 |
MOD_CK2_1 | 506 | 512 | PF00069 | 0.757 |
MOD_CMANNOS | 395 | 398 | PF00535 | 0.521 |
MOD_CMANNOS | 411 | 414 | PF00535 | 0.588 |
MOD_Cter_Amidation | 239 | 242 | PF01082 | 0.696 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.602 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.691 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.692 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.690 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.625 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.597 |
MOD_GlcNHglycan | 449 | 453 | PF01048 | 0.680 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.584 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.649 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.709 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.754 |
MOD_N-GLC_1 | 84 | 89 | PF02516 | 0.543 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.649 |
MOD_NEK2_2 | 358 | 363 | PF00069 | 0.726 |
MOD_OFUCOSY | 272 | 278 | PF10250 | 0.548 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.508 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.761 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.678 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.780 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.724 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.545 |
MOD_Plk_1 | 506 | 512 | PF00069 | 0.718 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.548 |
MOD_Plk_2-3 | 508 | 514 | PF00069 | 0.625 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.579 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.791 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.625 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.780 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.623 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.584 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.609 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.741 |
TRG_DiLeu_BaLyEn_6 | 360 | 365 | PF01217 | 0.578 |
TRG_ER_diArg_1 | 153 | 156 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 399 | 402 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 430 | 432 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 89 | 92 | PF00400 | 0.515 |
TRG_NLS_Bipartite_1 | 430 | 444 | PF00514 | 0.606 |
TRG_NLS_MonoExtC_3 | 438 | 443 | PF00514 | 0.677 |
TRG_NLS_MonoExtN_4 | 436 | 443 | PF00514 | 0.671 |
TRG_Pf-PMV_PEXEL_1 | 363 | 367 | PF00026 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2A7 | Leptomonas seymouri | 55% | 100% |
A4HAK0 | Leishmania braziliensis | 75% | 100% |
A4I9P4 | Leishmania infantum | 99% | 100% |
E9B4Q8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q3B8 | Leishmania major | 89% | 100% |