An expanding group of Kinetoplastid proteins. Some members of this group have a hydrophobic C-terminal segment that might help membrane attachment
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: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9B5M3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.563 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 96 | 98 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.640 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.435 |
DOC_CKS1_1 | 109 | 114 | PF01111 | 0.287 |
DOC_CYCLIN_RxL_1 | 235 | 246 | PF00134 | 0.217 |
DOC_CYCLIN_yClb1_LxF_4 | 72 | 77 | PF00134 | 0.387 |
DOC_CYCLIN_yCln2_LP_2 | 365 | 371 | PF00134 | 0.354 |
DOC_MAPK_gen_1 | 375 | 384 | PF00069 | 0.293 |
DOC_PP1_RVXF_1 | 72 | 78 | PF00149 | 0.376 |
DOC_PP2B_LxvP_1 | 251 | 254 | PF13499 | 0.317 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.270 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.309 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.242 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.404 |
LIG_14-3-3_CanoR_1 | 119 | 128 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 186 | 192 | PF00244 | 0.246 |
LIG_14-3-3_CanoR_1 | 299 | 305 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 74 | 82 | PF00244 | 0.316 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.267 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.359 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.253 |
LIG_LIR_Apic_2 | 194 | 198 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 24 | 35 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 256 | 267 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 108 | 113 | PF02991 | 0.251 |
LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.314 |
LIG_PTB_Apo_2 | 34 | 41 | PF02174 | 0.309 |
LIG_PTB_Phospho_1 | 34 | 40 | PF10480 | 0.309 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.283 |
LIG_SH2_CRK | 82 | 86 | PF00017 | 0.303 |
LIG_SH2_NCK_1 | 228 | 232 | PF00017 | 0.287 |
LIG_SH2_NCK_1 | 82 | 86 | PF00017 | 0.303 |
LIG_SH2_STAP1 | 181 | 185 | PF00017 | 0.341 |
LIG_SH2_STAP1 | 82 | 86 | PF00017 | 0.303 |
LIG_SH2_STAT3 | 160 | 163 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.370 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.375 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.503 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.415 |
LIG_Sin3_3 | 281 | 288 | PF02671 | 0.279 |
LIG_SUMO_SIM_anti_2 | 2 | 9 | PF11976 | 0.407 |
LIG_TYR_ITIM | 257 | 262 | PF00017 | 0.324 |
LIG_TYR_ITIM | 80 | 85 | PF00017 | 0.238 |
MOD_CDK_SPxK_1 | 221 | 227 | PF00069 | 0.382 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.396 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.368 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.182 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.486 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.576 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.534 |
MOD_GlcNHglycan | 311 | 315 | PF01048 | 0.695 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.287 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.347 |
MOD_N-GLC_2 | 29 | 31 | PF02516 | 0.569 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.294 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.317 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.350 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.276 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.323 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.350 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.364 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.396 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.408 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.325 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.309 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.286 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.309 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.242 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.382 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.399 |
MOD_SUMO_rev_2 | 292 | 297 | PF00179 | 0.397 |
MOD_SUMO_rev_2 | 355 | 363 | PF00179 | 0.368 |
TRG_DiLeu_BaEn_2 | 339 | 345 | PF01217 | 0.376 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.341 |
TRG_ER_diArg_1 | 118 | 121 | PF00400 | 0.287 |
TRG_ER_diArg_1 | 401 | 404 | PF00400 | 0.658 |
TRG_Pf-PMV_PEXEL_1 | 126 | 130 | PF00026 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 159 | 163 | PF00026 | 0.509 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P716 | Leptomonas seymouri | 54% | 100% |
A0A0S4IPR4 | Bodo saltans | 34% | 89% |
A0A1X0PAB7 | Trypanosomatidae | 34% | 100% |
A0A3Q8IUY8 | Leishmania donovani | 84% | 100% |
E9AHS2 | Leishmania infantum | 84% | 100% |
Q4Q2B3 | Leishmania major | 82% | 100% |