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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9ASF7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.535 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 265 | 267 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.461 |
DEG_SPOP_SBC_1 | 325 | 329 | PF00917 | 0.551 |
DEG_SPOP_SBC_1 | 63 | 67 | PF00917 | 0.647 |
DOC_CKS1_1 | 281 | 286 | PF01111 | 0.452 |
DOC_CKS1_1 | 408 | 413 | PF01111 | 0.498 |
DOC_MAPK_DCC_7 | 326 | 335 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 293 | 302 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 326 | 335 | PF00069 | 0.537 |
DOC_MIT_MIM_1 | 261 | 270 | PF04212 | 0.530 |
DOC_SPAK_OSR1_1 | 8 | 12 | PF12202 | 0.455 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.491 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.347 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.431 |
LIG_14-3-3_CanoR_1 | 108 | 116 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 120 | 126 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 366 | 372 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 405 | 411 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 427 | 434 | PF00244 | 0.279 |
LIG_14-3-3_CanoR_1 | 439 | 446 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 44 | 51 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 88 | 94 | PF00244 | 0.575 |
LIG_Actin_WH2_2 | 233 | 250 | PF00022 | 0.451 |
LIG_Actin_WH2_2 | 263 | 280 | PF00022 | 0.351 |
LIG_AP2alpha_2 | 432 | 434 | PF02296 | 0.439 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.368 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.614 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.340 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.474 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.568 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.545 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.497 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.444 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.484 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.564 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.378 |
LIG_Integrin_isoDGR_2 | 435 | 437 | PF01839 | 0.463 |
LIG_LIR_Gen_1 | 211 | 221 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 429 | 434 | PF02991 | 0.426 |
LIG_PTB_Apo_2 | 3 | 10 | PF02174 | 0.495 |
LIG_Rb_LxCxE_1 | 245 | 261 | PF01857 | 0.470 |
LIG_SH2_STAP1 | 125 | 129 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.457 |
LIG_SH3_1 | 278 | 284 | PF00018 | 0.428 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.535 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.648 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.596 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.507 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.532 |
LIG_SUMO_SIM_anti_2 | 172 | 180 | PF11976 | 0.447 |
LIG_SUMO_SIM_anti_2 | 24 | 30 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 21 | 27 | PF11976 | 0.405 |
LIG_TRAF2_1 | 170 | 173 | PF00917 | 0.443 |
LIG_TYR_ITIM | 92 | 97 | PF00017 | 0.596 |
MOD_CDK_SPK_2 | 321 | 326 | PF00069 | 0.654 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.519 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.385 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.506 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.518 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.550 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.706 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.497 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.484 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.537 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.582 |
MOD_Cter_Amidation | 263 | 266 | PF01082 | 0.337 |
MOD_DYRK1A_RPxSP_1 | 321 | 325 | PF00069 | 0.616 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.464 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.424 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.793 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.470 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.658 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.342 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.410 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.496 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.476 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.482 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.686 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.623 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.607 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.717 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.664 |
MOD_N-GLC_1 | 319 | 324 | PF02516 | 0.699 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.425 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.392 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.384 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.498 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.461 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.536 |
MOD_OFUCOSY | 13 | 18 | PF10250 | 0.481 |
MOD_PIKK_1 | 148 | 154 | PF00454 | 0.522 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.434 |
MOD_PIKK_1 | 304 | 310 | PF00454 | 0.710 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.618 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.627 |
MOD_PK_1 | 339 | 345 | PF00069 | 0.489 |
MOD_PKA_1 | 316 | 322 | PF00069 | 0.508 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.477 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.645 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.298 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.535 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.614 |
MOD_PKB_1 | 437 | 445 | PF00069 | 0.502 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.422 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.519 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.447 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.405 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.635 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.347 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.568 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.726 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.711 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.568 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.430 |
MOD_SUMO_for_1 | 343 | 346 | PF00179 | 0.499 |
MOD_SUMO_for_1 | 39 | 42 | PF00179 | 0.480 |
MOD_SUMO_rev_2 | 127 | 132 | PF00179 | 0.546 |
TRG_DiLeu_BaLyEn_6 | 328 | 333 | PF01217 | 0.476 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.599 |
TRG_ER_diArg_1 | 437 | 440 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.463 |
TRG_NES_CRM1_1 | 191 | 205 | PF08389 | 0.342 |
TRG_Pf-PMV_PEXEL_1 | 361 | 365 | PF00026 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 439 | 444 | PF00026 | 0.492 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0I6 | Leptomonas seymouri | 56% | 94% |
A0A0S4JLZ1 | Bodo saltans | 24% | 71% |
A0A1X0P8C3 | Trypanosomatidae | 32% | 100% |
A0A3S5H814 | Leishmania donovani | 85% | 100% |
A4HNP8 | Leishmania braziliensis | 74% | 100% |
A4ICU7 | Leishmania infantum | 86% | 100% |
Q4Q238 | Leishmania major | 89% | 100% |
V5DRR0 | Trypanosoma cruzi | 33% | 100% |