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: 60 |
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: 7 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: E9AJZ9
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 | 448 | 452 | PF00656 | 0.441 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.642 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.642 |
CLV_PCSK_PC7_1 | 2 | 8 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.429 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.474 |
DEG_SPOP_SBC_1 | 546 | 550 | PF00917 | 0.412 |
DOC_CKS1_1 | 83 | 88 | PF01111 | 0.438 |
DOC_CYCLIN_yCln2_LP_2 | 83 | 89 | PF00134 | 0.437 |
DOC_MAPK_FxFP_2 | 371 | 374 | PF00069 | 0.400 |
DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.431 |
DOC_PP2B_LxvP_1 | 67 | 70 | PF13499 | 0.448 |
DOC_PP4_FxxP_1 | 371 | 374 | PF00568 | 0.400 |
DOC_PP4_FxxP_1 | 81 | 84 | PF00568 | 0.446 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.326 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 564 | 568 | PF00917 | 0.403 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.446 |
LIG_14-3-3_CanoR_1 | 169 | 178 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 205 | 215 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 528 | 536 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 575 | 581 | PF00244 | 0.449 |
LIG_BRCT_BRCA1_1 | 325 | 329 | PF00533 | 0.445 |
LIG_BRCT_BRCA1_1 | 380 | 384 | PF00533 | 0.349 |
LIG_BRCT_BRCA1_1 | 77 | 81 | PF00533 | 0.451 |
LIG_Clathr_ClatBox_1 | 270 | 274 | PF01394 | 0.329 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.687 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.662 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.608 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.273 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.387 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.462 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.408 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.407 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.433 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.391 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.474 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.763 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.387 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.438 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.476 |
LIG_FHA_2 | 511 | 517 | PF00498 | 0.376 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.457 |
LIG_LIR_Apic_2 | 78 | 84 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 221 | 227 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 393 | 402 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 221 | 225 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 356 | 361 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 393 | 399 | PF02991 | 0.512 |
LIG_PCNA_yPIPBox_3 | 96 | 107 | PF02747 | 0.252 |
LIG_PDZ_Class_2 | 608 | 613 | PF00595 | 0.672 |
LIG_SH2_CRK | 491 | 495 | PF00017 | 0.457 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.439 |
LIG_SH2_NCK_1 | 47 | 51 | PF00017 | 0.452 |
LIG_SH2_NCK_1 | 491 | 495 | PF00017 | 0.409 |
LIG_SH2_STAP1 | 361 | 365 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 47 | 51 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.430 |
LIG_SH3_1 | 5 | 11 | PF00018 | 0.432 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.419 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.480 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.436 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.428 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.432 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.459 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.430 |
LIG_SUMO_SIM_anti_2 | 251 | 256 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 136 | 145 | PF11976 | 0.664 |
LIG_SUMO_SIM_par_1 | 231 | 236 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 251 | 256 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 319 | 324 | PF11976 | 0.420 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.702 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.655 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.630 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.684 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.286 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.401 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.537 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.387 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.389 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.381 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.372 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.359 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.497 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.492 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.439 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.426 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.430 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.323 |
MOD_CK2_1 | 474 | 480 | PF00069 | 0.501 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.457 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.468 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.419 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.511 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.438 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.514 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.640 |
MOD_GlcNHglycan | 221 | 225 | PF01048 | 0.635 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.668 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.572 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.720 |
MOD_GlcNHglycan | 354 | 358 | PF01048 | 0.543 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.580 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.600 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.640 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.533 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.762 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.665 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.653 |
MOD_GlcNHglycan | 566 | 569 | PF01048 | 0.695 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.700 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.631 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.633 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.667 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.334 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.448 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.407 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.487 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.435 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.449 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.430 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.386 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.525 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.384 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.475 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.463 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.440 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.465 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.652 |
MOD_N-GLC_2 | 527 | 529 | PF02516 | 0.672 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.651 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.609 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.592 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.600 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.444 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.431 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.473 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.308 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.349 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.433 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.433 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.348 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.447 |
MOD_NEK2_2 | 215 | 220 | PF00069 | 0.382 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.659 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.413 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.425 |
MOD_PIKK_1 | 449 | 455 | PF00454 | 0.457 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.678 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.627 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.339 |
MOD_PKA_2 | 527 | 533 | PF00069 | 0.478 |
MOD_PKB_1 | 169 | 177 | PF00069 | 0.586 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.703 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.372 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.460 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.366 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.410 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.442 |
MOD_Plk_1 | 510 | 516 | PF00069 | 0.327 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.613 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.458 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.401 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.457 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.498 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.377 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.401 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.503 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.435 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.476 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.430 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.424 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.470 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.449 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.454 |
TRG_NES_CRM1_1 | 217 | 228 | PF08389 | 0.440 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P251 | Leptomonas seymouri | 24% | 100% |
A0A381M9M8 | Leishmania infantum | 87% | 100% |
A0A3S5H581 | Leishmania donovani | 86% | 100% |
A0A3S5H583 | Leishmania donovani | 86% | 100% |
A0A451EJW1 | Leishmania donovani | 86% | 100% |
A0A451EJW4 | Leishmania donovani | 86% | 100% |
A0A451EJW6 | Leishmania donovani | 23% | 86% |
A4H3T8 | Leishmania braziliensis | 68% | 100% |
A4H3T9 | Leishmania braziliensis | 68% | 100% |
A4H3U0 | Leishmania braziliensis | 66% | 100% |
A4H3U1 | Leishmania braziliensis | 66% | 100% |
A4HS14 | Leishmania infantum | 23% | 86% |
E9AK01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 86% |
Q9N852 | Leishmania major | 85% | 100% |
Q9N853 | Leishmania major | 86% | 100% |
Q9N856 | Leishmania major | 85% | 100% |
Q9XZX9 | Leishmania major | 23% | 86% |