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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4H4Y7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 64 | 68 | PF00656 | 0.623 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.393 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.417 |
CLV_PCSK_PC1ET2_1 | 155 | 157 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 481 | 483 | PF00082 | 0.456 |
CLV_PCSK_PC7_1 | 477 | 483 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.653 |
CLV_Separin_Metazoa | 360 | 364 | PF03568 | 0.667 |
DOC_MAPK_FxFP_2 | 238 | 241 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 155 | 161 | PF00069 | 0.616 |
DOC_MAPK_gen_1 | 424 | 434 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 155 | 163 | PF00069 | 0.505 |
DOC_MAPK_MEF2A_6 | 252 | 260 | PF00069 | 0.553 |
DOC_PP1_RVXF_1 | 56 | 63 | PF00149 | 0.437 |
DOC_PP4_FxxP_1 | 238 | 241 | PF00568 | 0.484 |
DOC_SPAK_OSR1_1 | 341 | 345 | PF12202 | 0.357 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.683 |
DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.610 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.559 |
LIG_14-3-3_CanoR_1 | 123 | 129 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 144 | 150 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 156 | 162 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 191 | 199 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 334 | 340 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 411 | 419 | PF00244 | 0.333 |
LIG_14-3-3_CanoR_1 | 58 | 63 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 85 | 93 | PF00244 | 0.631 |
LIG_APCC_ABBA_1 | 432 | 437 | PF00400 | 0.365 |
LIG_BRCT_BRCA1_1 | 448 | 452 | PF00533 | 0.365 |
LIG_BRCT_BRCA1_1 | 505 | 509 | PF00533 | 0.537 |
LIG_Clathr_ClatBox_1 | 399 | 403 | PF01394 | 0.421 |
LIG_deltaCOP1_diTrp_1 | 34 | 43 | PF00928 | 0.669 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.582 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.375 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.528 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.610 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.701 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.413 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.515 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.540 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.568 |
LIG_GBD_Chelix_1 | 365 | 373 | PF00786 | 0.482 |
LIG_HCF-1_HBM_1 | 405 | 408 | PF13415 | 0.421 |
LIG_Integrin_isoDGR_2 | 350 | 352 | PF01839 | 0.524 |
LIG_LIR_Gen_1 | 34 | 45 | PF02991 | 0.730 |
LIG_LIR_Gen_1 | 380 | 389 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 454 | 463 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 61 | 70 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 78 | 88 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 167 | 171 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 223 | 227 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 316 | 320 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.733 |
LIG_LIR_Nem_3 | 380 | 384 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 61 | 65 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 78 | 83 | PF02991 | 0.442 |
LIG_PCNA_yPIPBox_3 | 191 | 202 | PF02747 | 0.447 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.643 |
LIG_SH2_GRB2like | 317 | 320 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.336 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.476 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.573 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.399 |
LIG_TRAF2_1 | 353 | 356 | PF00917 | 0.601 |
LIG_WRC_WIRS_1 | 146 | 151 | PF05994 | 0.416 |
MOD_CDC14_SPxK_1 | 105 | 108 | PF00782 | 0.475 |
MOD_CDK_SPxK_1 | 102 | 108 | PF00069 | 0.473 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.673 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.405 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.287 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.579 |
MOD_Cter_Amidation | 153 | 156 | PF01082 | 0.479 |
MOD_GlcNHglycan | 130 | 134 | PF01048 | 0.495 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.483 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.545 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.675 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.637 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.753 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.704 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.592 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.445 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.578 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.651 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.612 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.658 |
MOD_LATS_1 | 490 | 496 | PF00433 | 0.374 |
MOD_N-GLC_1 | 123 | 128 | PF02516 | 0.649 |
MOD_N-GLC_1 | 161 | 166 | PF02516 | 0.598 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.612 |
MOD_N-GLC_1 | 254 | 259 | PF02516 | 0.480 |
MOD_N-GLC_1 | 412 | 417 | PF02516 | 0.421 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.686 |
MOD_N-GLC_1 | 492 | 497 | PF02516 | 0.516 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.576 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.608 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.528 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.609 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.563 |
MOD_PKA_1 | 155 | 161 | PF00069 | 0.506 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.558 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.452 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.582 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.676 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.500 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.533 |
MOD_Plk_1 | 332 | 338 | PF00069 | 0.363 |
MOD_Plk_1 | 492 | 498 | PF00069 | 0.491 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.537 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.394 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.473 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.560 |
MOD_SUMO_rev_2 | 147 | 157 | PF00179 | 0.523 |
TRG_DiLeu_BaLyEn_6 | 395 | 400 | PF01217 | 0.421 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.295 |
TRG_ER_diArg_1 | 475 | 477 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 479 | 482 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 504 | 507 | PF00400 | 0.568 |
TRG_NES_CRM1_1 | 364 | 377 | PF08389 | 0.582 |
TRG_NES_CRM1_1 | 423 | 437 | PF08389 | 0.197 |
TRG_Pf-PMV_PEXEL_1 | 113 | 118 | PF00026 | 0.659 |
TRG_Pf-PMV_PEXEL_1 | 363 | 367 | PF00026 | 0.599 |
TRG_Pf-PMV_PEXEL_1 | 398 | 403 | PF00026 | 0.307 |
TRG_Pf-PMV_PEXEL_1 | 424 | 428 | PF00026 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 58 | 63 | PF00026 | 0.640 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9I2 | Leptomonas seymouri | 70% | 99% |
A0A0S4ILP7 | Bodo saltans | 40% | 100% |
A0A1X0NPY0 | Trypanosomatidae | 49% | 100% |
A0A3R7KA86 | Trypanosoma rangeli | 49% | 100% |
A0A3S7WPU9 | Leishmania donovani | 85% | 100% |
C9ZUR3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AG73 | Leishmania infantum | 85% | 100% |
E9AL52 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QIQ2 | Leishmania major | 85% | 100% |
V5D8S1 | Trypanosoma cruzi | 48% | 100% |