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 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: E9AHS2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.584 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 96 | 98 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.631 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.445 |
DEG_SPOP_SBC_1 | 264 | 268 | PF00917 | 0.294 |
DOC_CKS1_1 | 109 | 114 | PF01111 | 0.337 |
DOC_CYCLIN_yClb1_LxF_4 | 72 | 77 | PF00134 | 0.427 |
DOC_MAPK_gen_1 | 375 | 384 | PF00069 | 0.332 |
DOC_MAPK_MEF2A_6 | 126 | 135 | PF00069 | 0.282 |
DOC_MAPK_MEF2A_6 | 52 | 60 | PF00069 | 0.289 |
DOC_PP1_RVXF_1 | 247 | 253 | PF00149 | 0.295 |
DOC_PP1_RVXF_1 | 72 | 78 | PF00149 | 0.418 |
DOC_PP2B_LxvP_1 | 330 | 333 | PF13499 | 0.450 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.327 |
DOC_USP7_UBL2_3 | 336 | 340 | PF12436 | 0.499 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.328 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.277 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.472 |
LIG_14-3-3_CanoR_1 | 119 | 128 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 299 | 305 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 308 | 316 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 74 | 82 | PF00244 | 0.332 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.287 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.389 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.355 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.444 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.426 |
LIG_LIR_Apic_2 | 194 | 198 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 24 | 35 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 256 | 265 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 108 | 113 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.312 |
LIG_NRP_CendR_1 | 397 | 399 | PF00754 | 0.457 |
LIG_PTB_Apo_2 | 34 | 41 | PF02174 | 0.389 |
LIG_PTB_Phospho_1 | 34 | 40 | PF10480 | 0.391 |
LIG_SH2_CRK | 82 | 86 | PF00017 | 0.358 |
LIG_SH2_NCK_1 | 82 | 86 | PF00017 | 0.358 |
LIG_SH2_STAP1 | 181 | 185 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 82 | 86 | PF00017 | 0.358 |
LIG_SH2_STAT3 | 160 | 163 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.395 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.389 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.554 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.429 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.488 |
LIG_SH3_4 | 336 | 343 | PF00018 | 0.495 |
LIG_SUMO_SIM_anti_2 | 2 | 8 | PF11976 | 0.425 |
LIG_SUMO_SIM_anti_2 | 203 | 208 | PF11976 | 0.299 |
LIG_SUMO_SIM_anti_2 | 283 | 289 | PF11976 | 0.296 |
LIG_SUMO_SIM_anti_2 | 380 | 386 | PF11976 | 0.370 |
LIG_SUMO_SIM_par_1 | 380 | 386 | PF11976 | 0.273 |
LIG_TRAF2_1 | 67 | 70 | PF00917 | 0.383 |
LIG_UBA3_1 | 287 | 296 | PF00899 | 0.393 |
MOD_CDK_SPxK_1 | 221 | 227 | PF00069 | 0.428 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.429 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.536 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.621 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.359 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.426 |
MOD_N-GLC_2 | 29 | 31 | PF02516 | 0.610 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.410 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.311 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.335 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.370 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.369 |
MOD_PKA_1 | 295 | 301 | PF00069 | 0.460 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.566 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.443 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.433 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.349 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.338 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.249 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.335 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.328 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.277 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.428 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.467 |
MOD_SUMO_rev_2 | 17 | 27 | PF00179 | 0.466 |
MOD_SUMO_rev_2 | 292 | 298 | PF00179 | 0.412 |
TRG_DiLeu_BaEn_2 | 22 | 28 | PF01217 | 0.414 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.364 |
TRG_ER_diArg_1 | 118 | 121 | PF00400 | 0.337 |
TRG_Pf-PMV_PEXEL_1 | 126 | 130 | PF00026 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 159 | 163 | PF00026 | 0.528 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P716 | Leptomonas seymouri | 54% | 100% |
A0A0S4IPR4 | Bodo saltans | 39% | 88% |
A0A1X0PAB7 | Trypanosomatidae | 30% | 100% |
A0A3Q8IUY8 | Leishmania donovani | 99% | 100% |
E9B5M3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q2B3 | Leishmania major | 89% | 100% |