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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H6Q2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.453 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 86 | 88 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.503 |
CLV_Separin_Metazoa | 373 | 377 | PF03568 | 0.309 |
DEG_APCC_DBOX_1 | 340 | 348 | PF00400 | 0.403 |
DEG_APCC_DBOX_1 | 364 | 372 | PF00400 | 0.470 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.538 |
DOC_CDC14_PxL_1 | 96 | 104 | PF14671 | 0.498 |
DOC_CYCLIN_RxL_1 | 127 | 139 | PF00134 | 0.517 |
DOC_CYCLIN_RxL_1 | 59 | 67 | PF00134 | 0.532 |
DOC_MAPK_gen_1 | 115 | 124 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 168 | 176 | PF00069 | 0.282 |
DOC_MAPK_gen_1 | 393 | 402 | PF00069 | 0.344 |
DOC_MAPK_HePTP_8 | 114 | 126 | PF00069 | 0.473 |
DOC_MAPK_MEF2A_6 | 115 | 124 | PF00069 | 0.461 |
DOC_MAPK_NFAT4_5 | 117 | 125 | PF00069 | 0.488 |
DOC_MAPK_RevD_3 | 383 | 398 | PF00069 | 0.430 |
DOC_USP7_UBL2_3 | 393 | 397 | PF12436 | 0.290 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.581 |
LIG_14-3-3_CanoR_1 | 361 | 365 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 370 | 378 | PF00244 | 0.489 |
LIG_Actin_WH2_2 | 225 | 243 | PF00022 | 0.532 |
LIG_APCC_ABBA_1 | 80 | 85 | PF00400 | 0.517 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.469 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.613 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.377 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.360 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.450 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.400 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.467 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.519 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.390 |
LIG_GBD_Chelix_1 | 175 | 183 | PF00786 | 0.472 |
LIG_LIR_Apic_2 | 39 | 45 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 238 | 247 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 54 | 65 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 93 | 103 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.396 |
LIG_MAD2 | 393 | 401 | PF02301 | 0.585 |
LIG_PDZ_Class_2 | 397 | 402 | PF00595 | 0.638 |
LIG_Pex14_1 | 188 | 192 | PF04695 | 0.424 |
LIG_SH2_CRK | 42 | 46 | PF00017 | 0.560 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.502 |
LIG_SH2_NCK_1 | 306 | 310 | PF00017 | 0.486 |
LIG_SH2_NCK_1 | 352 | 356 | PF00017 | 0.484 |
LIG_SH2_PTP2 | 57 | 60 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 306 | 310 | PF00017 | 0.486 |
LIG_SH2_STAT3 | 327 | 330 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.434 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.269 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.529 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.516 |
LIG_Sin3_3 | 257 | 264 | PF02671 | 0.473 |
LIG_SUMO_SIM_anti_2 | 255 | 263 | PF11976 | 0.517 |
LIG_SUMO_SIM_anti_2 | 286 | 291 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 244 | 250 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 99 | 105 | PF11976 | 0.501 |
LIG_TYR_ITIM | 94 | 99 | PF00017 | 0.401 |
LIG_UBA3_1 | 102 | 108 | PF00899 | 0.538 |
LIG_Vh1_VBS_1 | 192 | 210 | PF01044 | 0.255 |
MOD_CDC14_SPxK_1 | 16 | 19 | PF00782 | 0.468 |
MOD_CDK_SPxK_1 | 13 | 19 | PF00069 | 0.458 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.438 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.523 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.525 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.379 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.482 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.297 |
MOD_Cter_Amidation | 276 | 279 | PF01082 | 0.413 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.498 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.417 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.378 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.641 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.460 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.424 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.507 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.534 |
MOD_N-GLC_1 | 13 | 18 | PF02516 | 0.456 |
MOD_N-GLC_1 | 214 | 219 | PF02516 | 0.422 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.515 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.706 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.440 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.504 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.410 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.425 |
MOD_NEK2_2 | 297 | 302 | PF00069 | 0.494 |
MOD_NEK2_2 | 360 | 365 | PF00069 | 0.522 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.507 |
MOD_PIKK_1 | 208 | 214 | PF00454 | 0.417 |
MOD_PIKK_1 | 386 | 392 | PF00454 | 0.429 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.527 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.388 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.438 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.511 |
MOD_Plk_2-3 | 334 | 340 | PF00069 | 0.357 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.466 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.542 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.630 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.576 |
TRG_DiLeu_BaEn_1 | 266 | 271 | PF01217 | 0.431 |
TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.540 |
TRG_DiLeu_BaLyEn_6 | 346 | 351 | PF01217 | 0.470 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 60 | 62 | PF00400 | 0.461 |
TRG_NLS_MonoExtN_4 | 393 | 400 | PF00514 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 127 | 132 | PF00026 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 62 | 66 | PF00026 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVS3 | Leptomonas seymouri | 65% | 99% |
A0A0S4KKN0 | Bodo saltans | 32% | 100% |
A0A1X0NUU6 | Trypanosomatidae | 36% | 100% |
A0A3R7M4V0 | Trypanosoma rangeli | 36% | 100% |
A0A3S7WRS2 | Leishmania donovani | 80% | 100% |
A4HV37 | Leishmania infantum | 80% | 100% |
D0A7B4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 76% |
E9ANR8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QGV1 | Leishmania major | 80% | 100% |
V5BWJ3 | Trypanosoma cruzi | 36% | 100% |