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: Q4QHT7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 462 | 466 | PF00656 | 0.588 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 456 | 458 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.621 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 520 | 522 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 11 | 13 | PF00082 | 0.527 |
CLV_PCSK_PC1ET2_1 | 119 | 121 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 520 | 522 | PF00082 | 0.566 |
CLV_PCSK_PC7_1 | 115 | 121 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.548 |
DEG_APCC_DBOX_1 | 287 | 295 | PF00400 | 0.548 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.616 |
DEG_SCF_FBW7_1 | 316 | 322 | PF00400 | 0.671 |
DEG_SPOP_SBC_1 | 74 | 78 | PF00917 | 0.674 |
DOC_CKS1_1 | 316 | 321 | PF01111 | 0.672 |
DOC_CYCLIN_yCln2_LP_2 | 20 | 26 | PF00134 | 0.652 |
DOC_MAPK_gen_1 | 520 | 526 | PF00069 | 0.586 |
DOC_MAPK_RevD_3 | 443 | 457 | PF00069 | 0.614 |
DOC_PP2B_LxvP_1 | 20 | 23 | PF13499 | 0.674 |
DOC_PP2B_LxvP_1 | 445 | 448 | PF13499 | 0.606 |
DOC_PP4_FxxP_1 | 300 | 303 | PF00568 | 0.675 |
DOC_PP4_FxxP_1 | 374 | 377 | PF00568 | 0.656 |
DOC_PP4_MxPP_1 | 441 | 444 | PF00568 | 0.574 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.678 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.574 |
LIG_14-3-3_CanoR_1 | 259 | 263 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 438 | 442 | PF00244 | 0.559 |
LIG_Actin_WH2_2 | 88 | 104 | PF00022 | 0.583 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.627 |
LIG_EVH1_1 | 442 | 446 | PF00568 | 0.581 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.472 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.711 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.573 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.504 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.676 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.521 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.600 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.678 |
LIG_FHA_2 | 475 | 481 | PF00498 | 0.527 |
LIG_LIR_Apic_2 | 372 | 377 | PF02991 | 0.650 |
LIG_LIR_Gen_1 | 254 | 264 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 493 | 502 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 493 | 497 | PF02991 | 0.548 |
LIG_MYND_1 | 443 | 447 | PF01753 | 0.595 |
LIG_PDZ_Class_2 | 521 | 526 | PF00595 | 0.584 |
LIG_PDZ_Wminus1_1 | 524 | 526 | PF00595 | 0.631 |
LIG_PTAP_UEV_1 | 305 | 310 | PF05743 | 0.623 |
LIG_PTB_Apo_2 | 59 | 66 | PF02174 | 0.690 |
LIG_SH2_CRK | 367 | 371 | PF00017 | 0.594 |
LIG_SH2_CRK | 494 | 498 | PF00017 | 0.559 |
LIG_SH2_CRK | 98 | 102 | PF00017 | 0.556 |
LIG_SH2_NCK_1 | 432 | 436 | PF00017 | 0.592 |
LIG_SH2_PTP2 | 257 | 260 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 2 | 6 | PF00017 | 0.580 |
LIG_SH2_STAT3 | 191 | 194 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.542 |
LIG_SH3_2 | 444 | 449 | PF14604 | 0.656 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.679 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.616 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.639 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.643 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.641 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.629 |
LIG_SH3_3 | 509 | 515 | PF00018 | 0.651 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.662 |
LIG_SH3_CIN85_PxpxPR_1 | 444 | 449 | PF14604 | 0.656 |
LIG_TRAF2_1 | 139 | 142 | PF00917 | 0.565 |
LIG_TRAF2_1 | 252 | 255 | PF00917 | 0.535 |
LIG_TYR_ITIM | 365 | 370 | PF00017 | 0.599 |
LIG_TYR_ITIM | 492 | 497 | PF00017 | 0.551 |
LIG_UBA3_1 | 185 | 193 | PF00899 | 0.392 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.574 |
LIG_WW_2 | 443 | 446 | PF00397 | 0.592 |
LIG_WW_3 | 446 | 450 | PF00397 | 0.664 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.658 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.563 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.698 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.615 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.458 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.559 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.703 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.615 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.469 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.683 |
MOD_Cter_Amidation | 518 | 521 | PF01082 | 0.566 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.628 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.612 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.613 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.645 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.676 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.596 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.758 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.734 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.754 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.682 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.578 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.579 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.572 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.511 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.604 |
MOD_N-GLC_1 | 15 | 20 | PF02516 | 0.614 |
MOD_N-GLC_1 | 500 | 505 | PF02516 | 0.636 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.621 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.651 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.512 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.551 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.567 |
MOD_NEK2_2 | 75 | 80 | PF00069 | 0.677 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.447 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.706 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.434 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.643 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.683 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.592 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.478 |
MOD_Plk_1 | 449 | 455 | PF00069 | 0.672 |
MOD_Plk_2-3 | 474 | 480 | PF00069 | 0.555 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.475 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.567 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.656 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.513 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.698 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.720 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.635 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.639 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.724 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.573 |
MOD_SUMO_for_1 | 129 | 132 | PF00179 | 0.480 |
MOD_SUMO_rev_2 | 33 | 37 | PF00179 | 0.658 |
MOD_SUMO_rev_2 | 480 | 487 | PF00179 | 0.599 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.601 |
TRG_ENDOCYTIC_2 | 494 | 497 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.546 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 288 | 291 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 455 | 457 | PF00400 | 0.643 |
TRG_NLS_MonoCore_2 | 117 | 122 | PF00514 | 0.503 |
TRG_NLS_MonoExtN_4 | 115 | 122 | PF00514 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 151 | 156 | PF00026 | 0.569 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7J5 | Leptomonas seymouri | 42% | 100% |
A0A3Q8IBX4 | Leishmania donovani | 92% | 100% |
A4H5N6 | Leishmania braziliensis | 72% | 100% |
A4HU08 | Leishmania infantum | 92% | 100% |
E9AMT8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |