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: Q4Q3B8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.472 |
CLV_C14_Caspase3-7 | 499 | 503 | PF00656 | 0.608 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.496 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 547 | 551 | PF00082 | 0.538 |
DEG_SPOP_SBC_1 | 47 | 51 | PF00917 | 0.610 |
DOC_ANK_TNKS_1 | 298 | 305 | PF00023 | 0.537 |
DOC_CKS1_1 | 202 | 207 | PF01111 | 0.538 |
DOC_CKS1_1 | 480 | 485 | PF01111 | 0.645 |
DOC_CYCLIN_yCln2_LP_2 | 188 | 194 | PF00134 | 0.586 |
DOC_MAPK_FxFP_2 | 111 | 114 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 438 | 446 | PF00069 | 0.570 |
DOC_PP1_RVXF_1 | 114 | 120 | PF00149 | 0.450 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.605 |
DOC_PP4_FxxP_1 | 111 | 114 | PF00568 | 0.525 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.621 |
DOC_USP7_UBL2_3 | 547 | 551 | PF12436 | 0.538 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.648 |
LIG_14-3-3_CanoR_1 | 154 | 159 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 297 | 302 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 353 | 361 | PF00244 | 0.630 |
LIG_Actin_WH2_2 | 533 | 549 | PF00022 | 0.621 |
LIG_BIR_III_4 | 236 | 240 | PF00653 | 0.641 |
LIG_deltaCOP1_diTrp_1 | 394 | 400 | PF00928 | 0.406 |
LIG_deltaCOP1_diTrp_1 | 412 | 416 | PF00928 | 0.441 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.412 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.595 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.473 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.695 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.519 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.598 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.711 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.705 |
LIG_LIR_Apic_2 | 108 | 114 | PF02991 | 0.413 |
LIG_LIR_Apic_2 | 25 | 31 | PF02991 | 0.653 |
LIG_LIR_Apic_2 | 33 | 39 | PF02991 | 0.636 |
LIG_LIR_Apic_2 | 370 | 375 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 171 | 175 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.468 |
LIG_PCNA_yPIPBox_3 | 418 | 432 | PF02747 | 0.467 |
LIG_SH2_CRK | 36 | 40 | PF00017 | 0.585 |
LIG_SH2_NCK_1 | 36 | 40 | PF00017 | 0.643 |
LIG_SH2_NCK_1 | 372 | 376 | PF00017 | 0.538 |
LIG_SH2_PTP2 | 28 | 31 | PF00017 | 0.518 |
LIG_SH2_SRC | 428 | 431 | PF00017 | 0.468 |
LIG_SH2_STAT3 | 341 | 344 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.544 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.597 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.536 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.548 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.609 |
LIG_TRAF2_1 | 460 | 463 | PF00917 | 0.592 |
LIG_TRAF2_1 | 485 | 488 | PF00917 | 0.598 |
LIG_UBA3_1 | 169 | 176 | PF00899 | 0.532 |
LIG_UBA3_1 | 539 | 547 | PF00899 | 0.549 |
LIG_WRC_WIRS_1 | 86 | 91 | PF05994 | 0.401 |
LIG_WW_3 | 380 | 384 | PF00397 | 0.566 |
MOD_CDK_SPxK_1 | 156 | 162 | PF00069 | 0.539 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.548 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.608 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.469 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.618 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.705 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.705 |
MOD_CMANNOS | 397 | 400 | PF00535 | 0.404 |
MOD_CMANNOS | 413 | 416 | PF00535 | 0.516 |
MOD_Cter_Amidation | 239 | 242 | PF01082 | 0.590 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.539 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.620 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.554 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.598 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.558 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.473 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.578 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.614 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.566 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.688 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.717 |
MOD_N-GLC_1 | 84 | 89 | PF02516 | 0.421 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.540 |
MOD_NEK2_2 | 360 | 365 | PF00069 | 0.576 |
MOD_OFUCOSY | 272 | 278 | PF10250 | 0.420 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.393 |
MOD_PIKK_1 | 340 | 346 | PF00454 | 0.630 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.611 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.437 |
MOD_Plk_1 | 508 | 514 | PF00069 | 0.633 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.459 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.530 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.542 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.653 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.555 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.539 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.665 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.495 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.472 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.647 |
TRG_DiLeu_BaLyEn_6 | 362 | 367 | PF01217 | 0.426 |
TRG_ER_diArg_1 | 153 | 156 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 403 | 405 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 89 | 92 | PF00400 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 365 | 369 | PF00026 | 0.416 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2A7 | Leptomonas seymouri | 54% | 100% |
A0A3S7X7L7 | Leishmania donovani | 89% | 100% |
A4HAK0 | Leishmania braziliensis | 76% | 100% |
A4I9P4 | Leishmania infantum | 89% | 100% |
E9B4Q8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 99% |