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: 65 |
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 | yes | yes: 11, no: 8 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4H3T9
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 | 78 | 82 | PF00656 | 0.434 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.576 |
DEG_SPOP_SBC_1 | 258 | 262 | PF00917 | 0.363 |
DOC_CYCLIN_RxL_1 | 246 | 257 | PF00134 | 0.369 |
DOC_PP2B_LxvP_1 | 310 | 313 | PF13499 | 0.377 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.428 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.417 |
LIG_14-3-3_CanoR_1 | 116 | 124 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 438 | 446 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 479 | 487 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 88 | 94 | PF00244 | 0.502 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.571 |
LIG_BRCT_BRCA1_1 | 236 | 240 | PF00533 | 0.475 |
LIG_Clathr_ClatBox_1 | 181 | 185 | PF01394 | 0.344 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.468 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.325 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.430 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.496 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.371 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.344 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.414 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.514 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.404 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.502 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.432 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.461 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.434 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.449 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.471 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.403 |
LIG_IRF3_LxIS_1 | 32 | 39 | PF10401 | 0.333 |
LIG_LIR_Apic_2 | 398 | 404 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 280 | 288 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 304 | 313 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 132 | 136 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 304 | 310 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 42 | 46 | PF02991 | 0.443 |
LIG_PDZ_Class_2 | 517 | 522 | PF00595 | 0.707 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.489 |
LIG_SH2_CRK | 487 | 491 | PF00017 | 0.397 |
LIG_SH2_NCK_1 | 401 | 405 | PF00017 | 0.443 |
LIG_SH2_NCK_1 | 487 | 491 | PF00017 | 0.395 |
LIG_SH2_STAP1 | 46 | 50 | PF00017 | 0.459 |
LIG_SH2_STAT3 | 468 | 471 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.378 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.510 |
LIG_SUMO_SIM_anti_2 | 162 | 167 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 142 | 147 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 162 | 167 | PF11976 | 0.269 |
LIG_SUMO_SIM_par_1 | 209 | 214 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 230 | 235 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 47 | 56 | PF11976 | 0.476 |
LIG_WRC_WIRS_1 | 281 | 286 | PF05994 | 0.346 |
MOD_CDK_SPxxK_3 | 431 | 438 | PF00069 | 0.417 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.381 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.422 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.497 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.435 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.396 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.397 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.365 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.372 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.391 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.467 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.513 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.421 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.429 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.524 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.428 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.447 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.444 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.681 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.527 |
MOD_GlcNHglycan | 132 | 136 | PF01048 | 0.643 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.675 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.620 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.675 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.582 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.672 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.613 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.726 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.600 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.645 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.711 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.631 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.656 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.568 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.386 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.465 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.344 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.451 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.423 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.608 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.484 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.446 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.409 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.498 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.505 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.525 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.493 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.455 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.509 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.448 |
MOD_N-GLC_1 | 140 | 145 | PF02516 | 0.674 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.436 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.366 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.444 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.469 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.383 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.459 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.492 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.367 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.431 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.430 |
MOD_PIKK_1 | 326 | 332 | PF00454 | 0.386 |
MOD_PIKK_1 | 410 | 416 | PF00454 | 0.404 |
MOD_PIKK_1 | 437 | 443 | PF00454 | 0.398 |
MOD_PIKK_1 | 467 | 473 | PF00454 | 0.412 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.493 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.415 |
MOD_PK_1 | 26 | 32 | PF00069 | 0.465 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.358 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.514 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.353 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.445 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.495 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.511 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.322 |
MOD_Plk_2-3 | 28 | 34 | PF00069 | 0.366 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.479 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.396 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.502 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.391 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.409 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.337 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.404 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.499 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.458 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.400 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.382 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.418 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.430 |
TRG_NES_CRM1_1 | 128 | 139 | PF08389 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P251 | Leptomonas seymouri | 22% | 100% |
A0A381M9M8 | Leishmania infantum | 69% | 99% |
A0A3S5H581 | Leishmania donovani | 69% | 99% |
A0A3S5H583 | Leishmania donovani | 69% | 99% |
A0A451EJW1 | Leishmania donovani | 69% | 99% |
A0A451EJW4 | Leishmania donovani | 69% | 99% |
A0A451EJW6 | Leishmania donovani | 24% | 74% |
A4H3T7 | Leishmania braziliensis | 99% | 100% |
A4H3T8 | Leishmania braziliensis | 99% | 100% |
A4H3U0 | Leishmania braziliensis | 94% | 100% |
A4H3U1 | Leishmania braziliensis | 94% | 100% |
A4HS14 | Leishmania infantum | 24% | 74% |
E9AJZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 85% |
E9AK01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 74% |
Q9N852 | Leishmania major | 69% | 100% |
Q9N853 | Leishmania major | 69% | 100% |
Q9N856 | Leishmania major | 68% | 100% |
Q9XZX9 | Leishmania major | 24% | 74% |