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: 1, no: 8 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4Q462
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 169 | 173 | PF00656 | 0.386 |
CLV_MEL_PAP_1 | 11 | 17 | PF00089 | 0.625 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.580 |
CLV_PCSK_FUR_1 | 262 | 266 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 264 | 266 | PF00082 | 0.438 |
CLV_PCSK_PC7_1 | 188 | 194 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.700 |
CLV_Separin_Metazoa | 121 | 125 | PF03568 | 0.368 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.445 |
DOC_ANK_TNKS_1 | 123 | 130 | PF00023 | 0.368 |
DOC_MAPK_gen_1 | 236 | 246 | PF00069 | 0.547 |
DOC_MAPK_gen_1 | 254 | 263 | PF00069 | 0.605 |
DOC_MAPK_MEF2A_6 | 19 | 26 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 254 | 263 | PF00069 | 0.633 |
DOC_PP2B_PxIxI_1 | 21 | 27 | PF00149 | 0.372 |
DOC_PP4_FxxP_1 | 302 | 305 | PF00568 | 0.606 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.501 |
DOC_USP7_UBL2_3 | 185 | 189 | PF12436 | 0.392 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.618 |
LIG_14-3-3_CanoR_1 | 265 | 271 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 27 | 33 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 289 | 297 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 34 | 42 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 6 | 10 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 77 | 86 | PF00244 | 0.385 |
LIG_Actin_WH2_2 | 119 | 136 | PF00022 | 0.403 |
LIG_AP2alpha_2 | 258 | 260 | PF02296 | 0.604 |
LIG_Clathr_ClatBox_1 | 83 | 87 | PF01394 | 0.368 |
LIG_deltaCOP1_diTrp_1 | 258 | 266 | PF00928 | 0.607 |
LIG_eIF4E_1 | 217 | 223 | PF01652 | 0.395 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.409 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.406 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.561 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.401 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.416 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.442 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.392 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.584 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.391 |
LIG_LIR_Apic_2 | 299 | 305 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 257 | 266 | PF02991 | 0.622 |
LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.532 |
LIG_PCNA_yPIPBox_3 | 115 | 126 | PF02747 | 0.368 |
LIG_SH2_GRB2like | 209 | 212 | PF00017 | 0.447 |
LIG_SH2_SRC | 209 | 212 | PF00017 | 0.447 |
LIG_SH2_SRC | 85 | 88 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.352 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.369 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.431 |
LIG_SH3_5 | 128 | 132 | PF00018 | 0.377 |
LIG_SUMO_SIM_par_1 | 43 | 48 | PF11976 | 0.444 |
LIG_TRAF2_1 | 250 | 253 | PF00917 | 0.596 |
LIG_UBA3_1 | 174 | 179 | PF00899 | 0.377 |
LIG_WW_3 | 74 | 78 | PF00397 | 0.449 |
MOD_CDC14_SPxK_1 | 205 | 208 | PF00782 | 0.385 |
MOD_CDK_SPxK_1 | 202 | 208 | PF00069 | 0.392 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.436 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.603 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.584 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.514 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.428 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.483 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.445 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.466 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.593 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.418 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.444 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.642 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.635 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.711 |
MOD_GlcNHglycan | 87 | 91 | PF01048 | 0.585 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.413 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.407 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.609 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.476 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.440 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.390 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.639 |
MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.624 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.427 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.424 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.674 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.458 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.471 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.453 |
MOD_NEK2_2 | 231 | 236 | PF00069 | 0.521 |
MOD_PKA_1 | 264 | 270 | PF00069 | 0.639 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.626 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.603 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.599 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.462 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.320 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.663 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.336 |
MOD_Plk_2-3 | 166 | 172 | PF00069 | 0.341 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.667 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.485 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.535 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.376 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.319 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.392 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.615 |
MOD_SUMO_rev_2 | 102 | 111 | PF00179 | 0.347 |
TRG_DiLeu_BaLyEn_6 | 19 | 24 | PF01217 | 0.423 |
TRG_ER_diArg_1 | 104 | 107 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 191 | 193 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 196 | 198 | PF00400 | 0.371 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4F7 | Leptomonas seymouri | 80% | 100% |
A0A0S4JAA8 | Bodo saltans | 57% | 100% |
A0A1X0P101 | Trypanosomatidae | 74% | 99% |
A0A3Q8IHR6 | Leishmania donovani | 96% | 100% |
A4HLI3 | Leishmania braziliensis | 89% | 100% |
A4I8Z3 | Leishmania infantum | 96% | 100% |
D0A4Z1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
E9B3W2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |