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. | yes | yes: 5 |
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: 16 |
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:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HB29
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.520 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 173 | 175 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.479 |
DEG_APCC_DBOX_1 | 211 | 219 | PF00400 | 0.464 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.616 |
DEG_SCF_FBW7_2 | 59 | 65 | PF00400 | 0.497 |
DOC_CKS1_1 | 322 | 327 | PF01111 | 0.544 |
DOC_CKS1_1 | 338 | 343 | PF01111 | 0.486 |
DOC_CKS1_1 | 59 | 64 | PF01111 | 0.495 |
DOC_CYCLIN_RxL_1 | 358 | 367 | PF00134 | 0.505 |
DOC_CYCLIN_RxL_1 | 373 | 383 | PF00134 | 0.439 |
DOC_MAPK_gen_1 | 118 | 128 | PF00069 | 0.456 |
DOC_MAPK_gen_1 | 19 | 30 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 85 | 92 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 23 | 32 | PF00069 | 0.495 |
DOC_PP1_RVXF_1 | 211 | 218 | PF00149 | 0.526 |
DOC_PP1_RVXF_1 | 67 | 73 | PF00149 | 0.528 |
DOC_PP4_FxxP_1 | 114 | 117 | PF00568 | 0.577 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.632 |
DOC_USP7_UBL2_3 | 173 | 177 | PF12436 | 0.358 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.436 |
LIG_14-3-3_CanoR_1 | 131 | 137 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 152 | 156 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 19 | 23 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 212 | 218 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 264 | 271 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 35 | 44 | PF00244 | 0.422 |
LIG_APCC_ABBA_1 | 96 | 101 | PF00400 | 0.597 |
LIG_APCC_ABBAyCdc20_2 | 95 | 101 | PF00400 | 0.595 |
LIG_BRCT_BRCA1_1 | 25 | 29 | PF00533 | 0.403 |
LIG_BRCT_BRCA1_1 | 286 | 290 | PF00533 | 0.394 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.481 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.521 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.565 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.748 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.484 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.588 |
LIG_FHA_2 | 19 | 25 | PF00498 | 0.453 |
LIG_Integrin_RGD_1 | 174 | 176 | PF01839 | 0.586 |
LIG_LIR_Apic_2 | 113 | 117 | PF02991 | 0.565 |
LIG_LIR_Apic_2 | 337 | 341 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 176 | 183 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 200 | 210 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 26 | 37 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 9 | 18 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 26 | 32 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 9 | 13 | PF02991 | 0.342 |
LIG_LRP6_Inhibitor_1 | 363 | 369 | PF00058 | 0.522 |
LIG_Pex14_2 | 18 | 22 | PF04695 | 0.425 |
LIG_REV1ctd_RIR_1 | 15 | 24 | PF16727 | 0.438 |
LIG_RPA_C_Fungi | 30 | 42 | PF08784 | 0.614 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.555 |
LIG_SH2_STAP1 | 178 | 182 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 37 | 41 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.524 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.667 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.478 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.567 |
LIG_SUMO_SIM_anti_2 | 133 | 138 | PF11976 | 0.326 |
LIG_SUMO_SIM_anti_2 | 9 | 16 | PF11976 | 0.373 |
LIG_SUMO_SIM_par_1 | 306 | 315 | PF11976 | 0.507 |
LIG_UBA3_1 | 28 | 33 | PF00899 | 0.546 |
MOD_CDK_SPK_2 | 58 | 63 | PF00069 | 0.493 |
MOD_CDK_SPK_2 | 90 | 95 | PF00069 | 0.434 |
MOD_CDK_SPxK_1 | 79 | 85 | PF00069 | 0.504 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.461 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.492 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.536 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.714 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.372 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.437 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.438 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.678 |
MOD_GlcNHglycan | 222 | 226 | PF01048 | 0.573 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.729 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.500 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.622 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.681 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.598 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.459 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.397 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.424 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.551 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.446 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.562 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.408 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.471 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.494 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.369 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.421 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.524 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.415 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.606 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.758 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.599 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.467 |
MOD_NEK2_2 | 197 | 202 | PF00069 | 0.541 |
MOD_NEK2_2 | 356 | 361 | PF00069 | 0.418 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.389 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.622 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.466 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.552 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.470 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.492 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.394 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.405 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.450 |
MOD_Plk_1 | 379 | 385 | PF00069 | 0.352 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.614 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.604 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.453 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.416 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.632 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.408 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.587 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.740 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.520 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.519 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.581 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.440 |
MOD_SUMO_for_1 | 348 | 351 | PF00179 | 0.411 |
MOD_SUMO_for_1 | 62 | 65 | PF00179 | 0.498 |
MOD_SUMO_rev_2 | 101 | 108 | PF00179 | 0.513 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.427 |
TRG_NES_CRM1_1 | 278 | 292 | PF08389 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 141 | 145 | PF00026 | 0.595 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P515 | Leptomonas seymouri | 66% | 100% |
A0A0S4J2A2 | Bodo saltans | 32% | 100% |
A0A1X0PA56 | Trypanosomatidae | 47% | 100% |
A0A3Q8IHQ1 | Leishmania donovani | 78% | 100% |
A0A3R7KID6 | Trypanosoma rangeli | 48% | 100% |
A4IA86 | Leishmania infantum | 78% | 100% |
C9ZM18 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9B599 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4Q2N4 | Leishmania major | 78% | 100% |
V5BKV3 | Trypanosoma cruzi | 48% | 100% |