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: 50 |
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: 3 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4H3T8
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_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.698 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.648 |
DEG_SPOP_SBC_1 | 310 | 314 | PF00917 | 0.371 |
DOC_CYCLIN_RxL_1 | 298 | 309 | PF00134 | 0.374 |
DOC_PP2B_LxvP_1 | 362 | 365 | PF13499 | 0.387 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.401 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.298 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.434 |
LIG_14-3-3_CanoR_1 | 140 | 146 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 168 | 176 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 490 | 498 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 529 | 537 | PF00244 | 0.452 |
LIG_BRCT_BRCA1_1 | 288 | 292 | PF00533 | 0.472 |
LIG_Clathr_ClatBox_1 | 233 | 237 | PF01394 | 0.346 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.441 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.483 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.339 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.381 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.661 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.379 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.346 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.411 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.524 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.519 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.356 |
LIG_FHA_2 | 336 | 342 | PF00498 | 0.472 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.451 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.479 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.663 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.386 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.451 |
LIG_LIR_Apic_2 | 450 | 456 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 332 | 340 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 356 | 365 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 184 | 188 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 332 | 337 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 356 | 362 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.504 |
LIG_PDZ_Class_2 | 567 | 572 | PF00595 | 0.728 |
LIG_SH2_CRK | 453 | 457 | PF00017 | 0.390 |
LIG_SH2_CRK | 537 | 541 | PF00017 | 0.407 |
LIG_SH2_NCK_1 | 453 | 457 | PF00017 | 0.383 |
LIG_SH2_NCK_1 | 537 | 541 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 98 | 102 | PF00017 | 0.478 |
LIG_SH2_STAT3 | 518 | 521 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.658 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 518 | 521 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.480 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.521 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.640 |
LIG_SUMO_SIM_anti_2 | 214 | 219 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 194 | 199 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 261 | 266 | PF11976 | 0.350 |
LIG_SUMO_SIM_par_1 | 282 | 287 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 99 | 108 | PF11976 | 0.495 |
LIG_WRC_WIRS_1 | 333 | 338 | PF05994 | 0.356 |
MOD_CDK_SPxxK_3 | 483 | 490 | PF00069 | 0.436 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.438 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.654 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.393 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.430 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.362 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.488 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.426 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.373 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.379 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.396 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.452 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.381 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.456 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.532 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.546 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.452 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.458 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.643 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.676 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.582 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.691 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.531 |
MOD_GlcNHglycan | 184 | 188 | PF01048 | 0.679 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.706 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.630 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.506 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.675 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.620 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.711 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.615 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.464 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.729 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.635 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.478 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.500 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.381 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.654 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.383 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.396 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.462 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.494 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.493 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.488 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.394 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.511 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.513 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.556 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.474 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.497 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.460 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.522 |
MOD_N-GLC_1 | 192 | 197 | PF02516 | 0.686 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.410 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.376 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.381 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.471 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.489 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.415 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.435 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.474 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.391 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.487 |
MOD_PIKK_1 | 116 | 122 | PF00454 | 0.507 |
MOD_PIKK_1 | 148 | 154 | PF00454 | 0.373 |
MOD_PIKK_1 | 30 | 36 | PF00454 | 0.659 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.391 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.406 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.422 |
MOD_PIKK_1 | 517 | 523 | PF00454 | 0.417 |
MOD_PK_1 | 78 | 84 | PF00069 | 0.412 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.468 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.654 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.393 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.545 |
MOD_PKA_2 | 528 | 534 | PF00069 | 0.357 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.502 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.533 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.409 |
MOD_Plk_2-3 | 80 | 86 | PF00069 | 0.378 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.407 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.494 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.371 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.483 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.473 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.394 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.337 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.478 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.520 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.501 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.389 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.436 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.432 |
TRG_NES_CRM1_1 | 180 | 191 | PF08389 | 0.485 |
TRG_NLS_MonoCore_2 | 3 | 8 | PF00514 | 0.650 |
TRG_NLS_MonoExtN_4 | 2 | 9 | PF00514 | 0.650 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A381M9M8 | Leishmania infantum | 69% | 100% |
A0A3S5H581 | Leishmania donovani | 68% | 100% |
A0A3S5H583 | Leishmania donovani | 69% | 100% |
A0A451EJW1 | Leishmania donovani | 68% | 100% |
A0A451EJW4 | Leishmania donovani | 68% | 100% |
A4H3T9 | Leishmania braziliensis | 99% | 100% |
A4H3U0 | Leishmania braziliensis | 94% | 100% |
A4H3U1 | Leishmania braziliensis | 94% | 100% |
E9AJZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 93% |
Q9N852 | Leishmania major | 69% | 100% |
Q9N853 | Leishmania major | 68% | 100% |
Q9N856 | Leishmania major | 68% | 100% |
Q9XZX9 | Leishmania major | 23% | 81% |