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: A4H8N4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 100 | 104 | PF00656 | 0.601 |
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.599 |
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.715 |
CLV_C14_Caspase3-7 | 360 | 364 | PF00656 | 0.824 |
CLV_C14_Caspase3-7 | 79 | 83 | PF00656 | 0.727 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.818 |
CLV_NRD_NRD_1 | 559 | 561 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 589 | 591 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.584 |
CLV_PCSK_FUR_1 | 258 | 262 | PF00082 | 0.813 |
CLV_PCSK_FUR_1 | 48 | 52 | PF00082 | 0.813 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.773 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.813 |
CLV_PCSK_KEX2_1 | 559 | 561 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 589 | 591 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.584 |
CLV_PCSK_PC1ET2_1 | 220 | 222 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.826 |
CLV_PCSK_PC1ET2_1 | 478 | 480 | PF00082 | 0.685 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.583 |
DEG_SPOP_SBC_1 | 570 | 574 | PF00917 | 0.567 |
DOC_ANK_TNKS_1 | 386 | 393 | PF00023 | 0.569 |
DOC_CYCLIN_yCln2_LP_2 | 458 | 464 | PF00134 | 0.577 |
DOC_MAPK_gen_1 | 559 | 565 | PF00069 | 0.714 |
DOC_PP1_RVXF_1 | 444 | 451 | PF00149 | 0.569 |
DOC_PP2B_LxvP_1 | 458 | 461 | PF13499 | 0.575 |
DOC_PP4_FxxP_1 | 540 | 543 | PF00568 | 0.571 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.571 |
DOC_PP4_MxPP_1 | 506 | 509 | PF00568 | 0.549 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.849 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 570 | 574 | PF00917 | 0.567 |
DOC_USP7_MATH_2 | 17 | 23 | PF00917 | 0.587 |
DOC_USP7_MATH_2 | 231 | 237 | PF00917 | 0.748 |
DOC_USP7_UBL2_3 | 478 | 482 | PF12436 | 0.681 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.786 |
LIG_14-3-3_CanoR_1 | 273 | 282 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 491 | 497 | PF00244 | 0.815 |
LIG_14-3-3_CanoR_1 | 559 | 566 | PF00244 | 0.788 |
LIG_deltaCOP1_diTrp_1 | 530 | 540 | PF00928 | 0.571 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.567 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.825 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.761 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.644 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.552 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.569 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.676 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.866 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.584 |
LIG_Integrin_RGD_1 | 101 | 103 | PF01839 | 0.609 |
LIG_Integrin_RGD_1 | 389 | 391 | PF01839 | 0.571 |
LIG_LIR_Apic_2 | 530 | 536 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 33 | 40 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 404 | 412 | PF02991 | 0.583 |
LIG_LIR_Gen_1 | 492 | 502 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 404 | 410 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 492 | 497 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.798 |
LIG_PROFILIN_1 | 2 | 8 | PF00235 | 0.567 |
LIG_SH2_CRK | 407 | 411 | PF00017 | 0.590 |
LIG_SH2_STAP1 | 207 | 211 | PF00017 | 0.586 |
LIG_SH2_STAP1 | 234 | 238 | PF00017 | 0.821 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.595 |
LIG_SH2_STAT3 | 421 | 424 | PF00017 | 0.582 |
LIG_SH2_STAT3 | 75 | 78 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.580 |
LIG_SH3_1 | 221 | 227 | PF00018 | 0.849 |
LIG_SH3_2 | 585 | 590 | PF14604 | 0.816 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.826 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.628 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.829 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.798 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.586 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.799 |
LIG_SH3_3 | 502 | 508 | PF00018 | 0.802 |
LIG_SH3_3 | 512 | 518 | PF00018 | 0.643 |
LIG_SH3_3 | 539 | 545 | PF00018 | 0.606 |
LIG_SH3_3 | 582 | 588 | PF00018 | 0.817 |
LIG_SUMO_SIM_par_1 | 16 | 22 | PF11976 | 0.590 |
LIG_TRAF2_1 | 176 | 179 | PF00917 | 0.591 |
LIG_TYR_ITSM | 490 | 497 | PF00017 | 0.559 |
LIG_WRC_WIRS_1 | 57 | 62 | PF05994 | 0.555 |
MOD_CDC14_SPxK_1 | 171 | 174 | PF00782 | 0.710 |
MOD_CDK_SPxK_1 | 168 | 174 | PF00069 | 0.705 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.711 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.690 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.578 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.721 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.798 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.785 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.741 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.716 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.597 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.723 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.586 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.582 |
MOD_CK2_1 | 558 | 564 | PF00069 | 0.827 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.551 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.776 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.712 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.819 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.698 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.666 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.785 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.650 |
MOD_GlcNHglycan | 431 | 435 | PF01048 | 0.572 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.629 |
MOD_GlcNHglycan | 567 | 571 | PF01048 | 0.780 |
MOD_GlcNHglycan | 89 | 93 | PF01048 | 0.738 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.624 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.716 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.690 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.601 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.692 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.810 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.562 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.574 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.572 |
MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.857 |
MOD_N-GLC_1 | 453 | 458 | PF02516 | 0.575 |
MOD_N-GLC_1 | 489 | 494 | PF02516 | 0.817 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.610 |
MOD_NEK2_2 | 108 | 113 | PF00069 | 0.594 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.532 |
MOD_PIKK_1 | 558 | 564 | PF00454 | 0.686 |
MOD_PKA_1 | 469 | 475 | PF00069 | 0.698 |
MOD_PKA_1 | 478 | 484 | PF00069 | 0.726 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.808 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.737 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.593 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.586 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.619 |
MOD_PKA_2 | 490 | 496 | PF00069 | 0.642 |
MOD_PKA_2 | 558 | 564 | PF00069 | 0.827 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.602 |
MOD_Plk_1 | 182 | 188 | PF00069 | 0.590 |
MOD_Plk_1 | 453 | 459 | PF00069 | 0.688 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.558 |
MOD_Plk_2-3 | 398 | 404 | PF00069 | 0.586 |
MOD_Plk_2-3 | 525 | 531 | PF00069 | 0.566 |
MOD_Plk_2-3 | 58 | 64 | PF00069 | 0.587 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.813 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.653 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.703 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.628 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.610 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.722 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.580 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.591 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.785 |
TRG_DiLeu_BaEn_1 | 35 | 40 | PF01217 | 0.652 |
TRG_DiLeu_BaLyEn_6 | 432 | 437 | PF01217 | 0.569 |
TRG_DiLeu_LyEn_5 | 35 | 40 | PF01217 | 0.505 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.762 |
TRG_ENDOCYTIC_2 | 407 | 410 | PF00928 | 0.596 |
TRG_ENDOCYTIC_2 | 494 | 497 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 599 | 602 | PF00928 | 0.551 |
TRG_ER_diArg_1 | 247 | 249 | PF00400 | 0.721 |
TRG_ER_diArg_1 | 386 | 389 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 469 | 471 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 48 | 51 | PF00400 | 0.796 |
TRG_ER_diArg_1 | 588 | 590 | PF00400 | 0.559 |
TRG_NLS_MonoCore_2 | 476 | 481 | PF00514 | 0.578 |
TRG_NLS_MonoExtC_3 | 477 | 482 | PF00514 | 0.672 |
TRG_NLS_MonoExtN_4 | 477 | 482 | PF00514 | 0.755 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IDQ3 | Leishmania donovani | 51% | 95% |
A4HX04 | Leishmania infantum | 52% | 96% |
E9AQR7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 94% |
Q4QEQ9 | Leishmania major | 51% | 100% |