A strange, fast-evolving receptor-like family of parazitic Kinetoplastids. While absent from many species, this family has expanded enormously on the Angomonas and Strigomonas lineages.. Very likely GPI-anchored protein. Very putatively might be involved in interactions with bacteria, explaining its expansion in symbiontic species.. Localization: Cell surface (by feature)
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: 40 |
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: 11, no: 1 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4H3T7
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0008233 | peptidase activity | 3 | 3 |
GO:0016787 | hydrolase activity | 2 | 3 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 136 | 140 | PF00656 | 0.625 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.581 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.455 |
DEG_SCF_FBW7_1 | 50 | 57 | PF00400 | 0.462 |
DEG_SPOP_SBC_1 | 316 | 320 | PF00917 | 0.385 |
DOC_CKS1_1 | 286 | 291 | PF01111 | 0.337 |
DOC_CYCLIN_RxL_1 | 304 | 315 | PF00134 | 0.385 |
DOC_CYCLIN_yCln2_LP_2 | 12 | 18 | PF00134 | 0.458 |
DOC_PP2B_LxvP_1 | 12 | 15 | PF13499 | 0.451 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.451 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.439 |
LIG_14-3-3_CanoR_1 | 146 | 152 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 174 | 182 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 32 | 41 | PF00244 | 0.456 |
LIG_BRCT_BRCA1_1 | 294 | 298 | PF00533 | 0.483 |
LIG_Clathr_ClatBox_1 | 239 | 243 | PF01394 | 0.356 |
LIG_CtBP_PxDLS_1 | 15 | 19 | PF00389 | 0.467 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.703 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.657 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.479 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.317 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.363 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.336 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.451 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.708 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.465 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.472 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.620 |
LIG_LIR_Gen_1 | 338 | 346 | PF02991 | 0.440 |
LIG_LIR_LC3C_4 | 288 | 292 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 100 | 104 | PF02991 | 0.683 |
LIG_LIR_Nem_3 | 190 | 194 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.471 |
LIG_MYND_1 | 10 | 14 | PF01753 | 0.439 |
LIG_MYND_1 | 48 | 52 | PF01753 | 0.453 |
LIG_SH2_STAP1 | 104 | 108 | PF00017 | 0.678 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.680 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.492 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.499 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.448 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.434 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.440 |
LIG_SUMO_SIM_anti_2 | 220 | 225 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 105 | 114 | PF11976 | 0.689 |
LIG_SUMO_SIM_par_1 | 13 | 19 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 200 | 205 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 220 | 225 | PF11976 | 0.277 |
LIG_SUMO_SIM_par_1 | 267 | 272 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 282 | 288 | PF11976 | 0.382 |
LIG_WRC_WIRS_1 | 339 | 344 | PF05994 | 0.410 |
LIG_WW_3 | 46 | 50 | PF00397 | 0.452 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.635 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.386 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.470 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.409 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.329 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.442 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.335 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.505 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.421 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.413 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.707 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.467 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.484 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.461 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.435 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.408 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.493 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.250 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.498 |
MOD_GlcNHglycan | 190 | 194 | PF01048 | 0.657 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.704 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.675 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.648 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.731 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.633 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.529 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.802 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.664 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.402 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.450 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.467 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.642 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.638 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.369 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.465 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.367 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.385 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.445 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.482 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.511 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.326 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.615 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.455 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.745 |
MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.682 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.450 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.701 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.566 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.697 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.640 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.470 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.479 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.392 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.441 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.637 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.660 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.696 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.366 |
MOD_PK_1 | 84 | 90 | PF00069 | 0.613 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.648 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.384 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.510 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.478 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.714 |
MOD_Plk_2-3 | 86 | 92 | PF00069 | 0.585 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.558 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.475 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.364 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.465 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.485 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.393 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.399 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.458 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.335 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.481 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.438 |
TRG_NES_CRM1_1 | 186 | 197 | PF08389 | 0.477 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A381M9M8 | Leishmania infantum | 76% | 69% |
A0A3S5H581 | Leishmania donovani | 75% | 69% |
A0A3S5H583 | Leishmania donovani | 75% | 69% |
A0A451EJW1 | Leishmania donovani | 75% | 69% |
A0A451EJW4 | Leishmania donovani | 75% | 69% |
A4H3T9 | Leishmania braziliensis | 99% | 69% |
A4H3U0 | Leishmania braziliensis | 97% | 69% |
A4H3U1 | Leishmania braziliensis | 97% | 69% |
Q9N852 | Leishmania major | 77% | 68% |
Q9N853 | Leishmania major | 77% | 68% |
Q9N856 | Leishmania major | 77% | 68% |