Uncharacterized Protein, Uncharacterized
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: 10 |
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:0110165 | cellular anatomical entity | 1 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HRL2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 151 | 155 | PF00656 | 0.538 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.570 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 117 | 119 | PF00082 | 0.548 |
CLV_PCSK_PC1ET2_1 | 351 | 353 | PF00082 | 0.606 |
CLV_PCSK_PC7_1 | 69 | 75 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.409 |
DEG_SPOP_SBC_1 | 321 | 325 | PF00917 | 0.522 |
DOC_CKS1_1 | 333 | 338 | PF01111 | 0.635 |
DOC_MAPK_gen_1 | 73 | 84 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 78 | 86 | PF00069 | 0.459 |
DOC_PP2B_LxvP_1 | 168 | 171 | PF13499 | 0.509 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.581 |
DOC_USP7_UBL2_3 | 29 | 33 | PF12436 | 0.512 |
DOC_USP7_UBL2_3 | 59 | 63 | PF12436 | 0.593 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.699 |
LIG_14-3-3_CanoR_1 | 223 | 230 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 73 | 82 | PF00244 | 0.491 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.492 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.442 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.355 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.578 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.526 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.478 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.537 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.611 |
LIG_Integrin_isoDGR_2 | 37 | 39 | PF01839 | 0.575 |
LIG_LIR_Gen_1 | 131 | 142 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 208 | 218 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 22 | 30 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 81 | 90 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 295 | 300 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 81 | 86 | PF02991 | 0.439 |
LIG_NRP_CendR_1 | 351 | 354 | PF00754 | 0.713 |
LIG_Pex14_2 | 293 | 297 | PF04695 | 0.431 |
LIG_SH2_NCK_1 | 161 | 165 | PF00017 | 0.358 |
LIG_SH2_SRC | 129 | 132 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.414 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.649 |
LIG_UBA3_1 | 17 | 23 | PF00899 | 0.390 |
LIG_UBA3_1 | 24 | 33 | PF00899 | 0.450 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.494 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.694 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.616 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.487 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.451 |
MOD_Cter_Amidation | 347 | 350 | PF01082 | 0.685 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.552 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.429 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.534 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.483 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.502 |
MOD_GlcNHglycan | 304 | 308 | PF01048 | 0.517 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.604 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.551 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.523 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.515 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.501 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.399 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.643 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.572 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.622 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.542 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.523 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.658 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.519 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.489 |
MOD_PIKK_1 | 272 | 278 | PF00454 | 0.523 |
MOD_PIKK_1 | 73 | 79 | PF00454 | 0.663 |
MOD_PK_1 | 78 | 84 | PF00069 | 0.565 |
MOD_PKA_1 | 69 | 75 | PF00069 | 0.571 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.496 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.425 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.579 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.551 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.442 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.550 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.549 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.699 |
TRG_DiLeu_BaEn_1 | 13 | 18 | PF01217 | 0.456 |
TRG_DiLeu_BaEn_4 | 13 | 19 | PF01217 | 0.477 |
TRG_ER_diArg_1 | 270 | 273 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 352 | 354 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.678 |
TRG_ER_diLys_1 | 349 | 354 | PF00400 | 0.663 |
TRG_NLS_MonoCore_2 | 348 | 353 | PF00514 | 0.707 |
TRG_NLS_MonoExtC_3 | 348 | 353 | PF00514 | 0.633 |
TRG_NLS_MonoExtC_3 | 61 | 67 | PF00514 | 0.630 |
TRG_NLS_MonoExtN_4 | 349 | 354 | PF00514 | 0.655 |
TRG_NLS_MonoExtN_4 | 59 | 66 | PF00514 | 0.646 |
TRG_Pf-PMV_PEXEL_1 | 111 | 116 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 9 | 13 | PF00026 | 0.444 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWM5 | Leptomonas seymouri | 60% | 100% |
A0A0S4JHT8 | Bodo saltans | 28% | 99% |
A0A1X0NKG5 | Trypanosomatidae | 37% | 90% |
A0A3S5H4Y1 | Leishmania donovani | 99% | 100% |
A0A422N6Z1 | Trypanosoma rangeli | 39% | 91% |
A4H3B2 | Leishmania braziliensis | 77% | 100% |
C9ZJ00 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 91% |
E9AC84 | Leishmania major | 89% | 99% |
E9AJH6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5B685 | Trypanosoma cruzi | 38% | 91% |