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: E9B271
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 116 | 120 | PF00656 | 0.763 |
CLV_C14_Caspase3-7 | 244 | 248 | PF00656 | 0.405 |
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.450 |
CLV_C14_Caspase3-7 | 97 | 101 | PF00656 | 0.406 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.522 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.501 |
CLV_PCSK_PC1ET2_1 | 456 | 458 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.282 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.517 |
DEG_ODPH_VHL_1 | 460 | 472 | PF01847 | 0.492 |
DOC_CKS1_1 | 475 | 480 | PF01111 | 0.417 |
DOC_MAPK_gen_1 | 183 | 191 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 281 | 290 | PF00069 | 0.309 |
DOC_MAPK_MEF2A_6 | 281 | 290 | PF00069 | 0.297 |
DOC_PP1_RVXF_1 | 185 | 192 | PF00149 | 0.352 |
DOC_PP1_RVXF_1 | 272 | 278 | PF00149 | 0.341 |
DOC_PP2B_LxvP_1 | 67 | 70 | PF13499 | 0.545 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.515 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.291 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.689 |
LIG_14-3-3_CanoR_1 | 142 | 147 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 340 | 344 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 529 | 535 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 56 | 66 | PF00244 | 0.737 |
LIG_BRCT_BRCA1_1 | 385 | 389 | PF00533 | 0.391 |
LIG_deltaCOP1_diTrp_1 | 215 | 223 | PF00928 | 0.393 |
LIG_deltaCOP1_diTrp_1 | 481 | 491 | PF00928 | 0.307 |
LIG_EVH1_2 | 316 | 320 | PF00568 | 0.461 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.522 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.300 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.348 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.510 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.425 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.468 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.571 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.387 |
LIG_Integrin_isoDGR_2 | 184 | 186 | PF01839 | 0.372 |
LIG_KLC1_Yacidic_2 | 151 | 156 | PF13176 | 0.473 |
LIG_LIR_Apic_2 | 499 | 504 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 151 | 162 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 175 | 181 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 293 | 298 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 386 | 397 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 411 | 419 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 71 | 81 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 232 | 238 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 293 | 297 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 411 | 417 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 467 | 473 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.420 |
LIG_MYND_1 | 471 | 475 | PF01753 | 0.295 |
LIG_Pex14_2 | 491 | 495 | PF04695 | 0.403 |
LIG_REV1ctd_RIR_1 | 275 | 285 | PF16727 | 0.335 |
LIG_SH2_CRK | 414 | 418 | PF00017 | 0.391 |
LIG_SH2_NCK_1 | 414 | 418 | PF00017 | 0.435 |
LIG_SH2_NCK_1 | 74 | 78 | PF00017 | 0.460 |
LIG_SH2_PTP2 | 154 | 157 | PF00017 | 0.373 |
LIG_SH2_SRC | 414 | 417 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.412 |
LIG_SH3_2 | 269 | 274 | PF14604 | 0.335 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.466 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.276 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.443 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.422 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.455 |
LIG_SUMO_SIM_par_1 | 94 | 100 | PF11976 | 0.448 |
LIG_TYR_ITSM | 410 | 417 | PF00017 | 0.417 |
MOD_CDC14_SPxK_1 | 271 | 274 | PF00782 | 0.385 |
MOD_CDK_SPK_2 | 383 | 388 | PF00069 | 0.397 |
MOD_CDK_SPxK_1 | 268 | 274 | PF00069 | 0.323 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.679 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.603 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.312 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.634 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.410 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.611 |
MOD_Cter_Amidation | 184 | 187 | PF01082 | 0.349 |
MOD_Cter_Amidation | 454 | 457 | PF01082 | 0.405 |
MOD_GlcNHglycan | 114 | 118 | PF01048 | 0.650 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.674 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.356 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.357 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.713 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.517 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.656 |
MOD_GlcNHglycan | 78 | 82 | PF01048 | 0.387 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.744 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.675 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.276 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.375 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.690 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.331 |
MOD_N-GLC_1 | 447 | 452 | PF02516 | 0.510 |
MOD_N-GLC_2 | 432 | 434 | PF02516 | 0.357 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.472 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.393 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.415 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.546 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.627 |
MOD_PK_1 | 142 | 148 | PF00069 | 0.631 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.617 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.414 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.386 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.313 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.724 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.498 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.477 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.238 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.331 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.685 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.455 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.291 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.468 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.389 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.410 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.685 |
MOD_SUMO_for_1 | 367 | 370 | PF00179 | 0.469 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.518 |
TRG_ER_diArg_1 | 186 | 188 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.603 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIU3 | Leptomonas seymouri | 71% | 99% |
A0A0S4JSP7 | Bodo saltans | 37% | 86% |
A0A3Q8ICS2 | Leishmania donovani | 94% | 100% |
A4HJR0 | Leishmania braziliensis | 84% | 100% |
A4I777 | Leishmania infantum | 94% | 100% |
C9ZWM7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
Q4Q5Y8 | Leishmania major | 93% | 100% |
V5BGM3 | Trypanosoma cruzi | 54% | 100% |