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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0005886 | plasma membrane | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4H4E9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.232 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.226 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.490 |
CLV_PCSK_FUR_1 | 223 | 227 | PF00082 | 0.243 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.176 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.243 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.226 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.484 |
CLV_PCSK_PC1ET2_1 | 198 | 200 | PF00082 | 0.243 |
CLV_PCSK_PC1ET2_1 | 225 | 227 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.459 |
CLV_Separin_Metazoa | 184 | 188 | PF03568 | 0.258 |
CLV_Separin_Metazoa | 209 | 213 | PF03568 | 0.258 |
DEG_APCC_DBOX_1 | 164 | 172 | PF00400 | 0.258 |
DEG_APCC_DBOX_1 | 2 | 10 | PF00400 | 0.412 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.511 |
DOC_CYCLIN_RxL_1 | 223 | 233 | PF00134 | 0.243 |
DOC_MAPK_gen_1 | 223 | 230 | PF00069 | 0.243 |
DOC_MAPK_gen_1 | 3 | 9 | PF00069 | 0.613 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.249 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.317 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.700 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.656 |
LIG_14-3-3_CanoR_1 | 165 | 169 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 175 | 179 | PF00244 | 0.302 |
LIG_14-3-3_CanoR_1 | 212 | 216 | PF00244 | 0.243 |
LIG_14-3-3_CanoR_1 | 59 | 63 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 79 | 85 | PF00244 | 0.129 |
LIG_Actin_WH2_2 | 119 | 135 | PF00022 | 0.243 |
LIG_APCC_ABBA_1 | 91 | 96 | PF00400 | 0.337 |
LIG_deltaCOP1_diTrp_1 | 85 | 94 | PF00928 | 0.277 |
LIG_EH1_1 | 199 | 207 | PF00400 | 0.388 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.324 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.462 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.337 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.661 |
LIG_LIR_Gen_1 | 340 | 349 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 61 | 67 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 86 | 95 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 310 | 315 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 340 | 345 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 61 | 66 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.243 |
LIG_PTB_Apo_2 | 143 | 150 | PF02174 | 0.243 |
LIG_SH2_STAT3 | 12 | 15 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.243 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.243 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.247 |
LIG_SUMO_SIM_anti_2 | 181 | 187 | PF11976 | 0.308 |
LIG_SUMO_SIM_anti_2 | 280 | 288 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 122 | 127 | PF11976 | 0.243 |
LIG_TRAF2_1 | 24 | 27 | PF00917 | 0.628 |
LIG_UBA3_1 | 130 | 139 | PF00899 | 0.243 |
LIG_WW_3 | 56 | 60 | PF00397 | 0.529 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.243 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.388 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.515 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.605 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.308 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.485 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.246 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.402 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.480 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.270 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.612 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.578 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.337 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.277 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.337 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.122 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.122 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.337 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.337 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.122 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.232 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.517 |
MOD_N-GLC_1 | 112 | 117 | PF02516 | 0.243 |
MOD_N-GLC_1 | 178 | 183 | PF02516 | 0.308 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.611 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.243 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.327 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.220 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.613 |
MOD_NEK2_2 | 155 | 160 | PF00069 | 0.243 |
MOD_NEK2_2 | 58 | 63 | PF00069 | 0.442 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.299 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.662 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.360 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.302 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.243 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.534 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.421 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.243 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.360 |
MOD_Plk_2-3 | 257 | 263 | PF00069 | 0.300 |
MOD_Plk_2-3 | 49 | 55 | PF00069 | 0.566 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.243 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.346 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.170 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.258 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.492 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.415 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.611 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.537 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.660 |
TRG_ER_diArg_1 | 186 | 188 | PF00400 | 0.277 |
TRG_ER_diArg_1 | 2 | 5 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.252 |
TRG_NES_CRM1_1 | 125 | 136 | PF08389 | 0.243 |
TRG_NLS_Bipartite_1 | 212 | 229 | PF00514 | 0.258 |
TRG_NLS_MonoCore_2 | 223 | 228 | PF00514 | 0.337 |
TRG_NLS_MonoExtN_4 | 223 | 229 | PF00514 | 0.243 |
TRG_Pf-PMV_PEXEL_1 | 226 | 231 | PF00026 | 0.243 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTU5 | Leptomonas seymouri | 84% | 99% |
A0A0S4INS2 | Bodo saltans | 61% | 100% |
A0A1X0NKE1 | Trypanosomatidae | 68% | 84% |
A0A3R7M6V7 | Trypanosoma rangeli | 62% | 93% |
A0A3S5H5L4 | Leishmania donovani | 93% | 100% |
A4HSM6 | Leishmania infantum | 93% | 100% |
C9ZND8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 66% | 67% |
E9AKL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9AS80 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
O60121 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 46% | 100% |
P0AA53 | Escherichia coli (strain K12) | 36% | 100% |
P0AA54 | Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) | 36% | 100% |
P0AA55 | Escherichia coli O157:H7 | 36% | 100% |
P0AA56 | Shigella flexneri | 36% | 100% |
P0DKS0 | Wigglesworthia glossinidia brevipalpis | 33% | 100% |
P63694 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 31% | 94% |
P72655 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 36% | 100% |
P9WPR8 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 31% | 94% |
P9WPR9 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 31% | 94% |
Q32LL2 | Bos taurus | 47% | 100% |
Q4FZT0 | Rattus norvegicus | 46% | 100% |
Q4QJ98 | Leishmania major | 93% | 100% |
Q99JB2 | Mus musculus | 46% | 100% |
Q9FHM7 | Arabidopsis thaliana | 23% | 100% |
Q9UJZ1 | Homo sapiens | 45% | 100% |
V5BBU5 | Trypanosoma cruzi | 68% | 88% |