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: 15 |
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4I5R1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 96 | 100 | PF00656 | 0.513 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.563 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.504 |
DEG_SPOP_SBC_1 | 35 | 39 | PF00917 | 0.568 |
DOC_MAPK_gen_1 | 107 | 116 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 297 | 307 | PF00069 | 0.398 |
DOC_PP1_RVXF_1 | 107 | 114 | PF00149 | 0.441 |
DOC_PP1_RVXF_1 | 130 | 137 | PF00149 | 0.413 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.558 |
DOC_USP7_UBL2_3 | 297 | 301 | PF12436 | 0.418 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.503 |
LIG_14-3-3_CanoR_1 | 107 | 112 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 115 | 120 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 132 | 137 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 163 | 171 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 20 | 28 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 249 | 253 | PF00244 | 0.567 |
LIG_APCC_ABBA_1 | 59 | 64 | PF00400 | 0.446 |
LIG_BRCT_BRCA1_1 | 109 | 113 | PF00533 | 0.527 |
LIG_deltaCOP1_diTrp_1 | 296 | 304 | PF00928 | 0.508 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.409 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.670 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.320 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.410 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.457 |
LIG_LIR_Gen_1 | 102 | 113 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 118 | 125 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 227 | 235 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 303 | 312 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 118 | 122 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 303 | 307 | PF02991 | 0.379 |
LIG_MLH1_MIPbox_1 | 109 | 113 | PF16413 | 0.527 |
LIG_NRBOX | 202 | 208 | PF00104 | 0.398 |
LIG_REV1ctd_RIR_1 | 110 | 119 | PF16727 | 0.493 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.433 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.426 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.524 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.291 |
LIG_TRAF2_1 | 166 | 169 | PF00917 | 0.477 |
LIG_TRAF2_2 | 137 | 142 | PF00917 | 0.497 |
LIG_WRC_WIRS_1 | 116 | 121 | PF05994 | 0.454 |
MOD_CDC14_SPxK_1 | 30 | 33 | PF00782 | 0.530 |
MOD_CDK_SPxK_1 | 27 | 33 | PF00069 | 0.511 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.497 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.483 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.457 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.453 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.465 |
MOD_GlcNHglycan | 291 | 296 | PF01048 | 0.560 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.519 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.619 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.465 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.528 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.465 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.382 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.540 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.428 |
MOD_NEK2_2 | 5 | 10 | PF00069 | 0.393 |
MOD_NEK2_2 | 62 | 67 | PF00069 | 0.422 |
MOD_PK_1 | 107 | 113 | PF00069 | 0.469 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.476 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.475 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.461 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.511 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.550 |
MOD_Plk_2-3 | 199 | 205 | PF00069 | 0.457 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.571 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.657 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.420 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.471 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.498 |
MOD_SUMO_for_1 | 217 | 220 | PF00179 | 0.461 |
MOD_SUMO_rev_2 | 13 | 17 | PF00179 | 0.478 |
MOD_SUMO_rev_2 | 259 | 265 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 267 | 275 | PF00179 | 0.592 |
TRG_DiLeu_BaEn_1 | 36 | 41 | PF01217 | 0.501 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.438 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8P9 | Leptomonas seymouri | 51% | 100% |
A0A3Q8II20 | Leishmania donovani | 100% | 100% |
A4HIG5 | Leishmania braziliensis | 68% | 100% |
E9B106 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q760 | Leishmania major | 89% | 97% |