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 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: Q9N853
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0008233 | peptidase activity | 3 | 4 |
GO:0016787 | hydrolase activity | 2 | 4 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 359 | 363 | PF00656 | 0.438 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.663 |
DOC_MAPK_FxFP_2 | 282 | 285 | PF00069 | 0.401 |
DOC_PP4_FxxP_1 | 282 | 285 | PF00568 | 0.401 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.504 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.557 |
LIG_14-3-3_CanoR_1 | 116 | 126 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 220 | 228 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 439 | 447 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 493 | 499 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 88 | 94 | PF00244 | 0.500 |
LIG_BRCT_BRCA1_1 | 236 | 240 | PF00533 | 0.437 |
LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.368 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.379 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.455 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.310 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.371 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.486 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.396 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.499 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.485 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.347 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.376 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.471 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.465 |
LIG_FHA_2 | 422 | 428 | PF00498 | 0.391 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.381 |
LIG_LIR_Gen_1 | 44 | 52 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 132 | 136 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 267 | 272 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 304 | 310 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.441 |
LIG_PDZ_Class_2 | 526 | 531 | PF00595 | 0.716 |
LIG_SH2_CRK | 46 | 50 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 272 | 276 | PF00017 | 0.317 |
LIG_SH2_STAP1 | 46 | 50 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.367 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.494 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.400 |
LIG_SUMO_SIM_anti_2 | 16 | 21 | PF11976 | 0.504 |
LIG_SUMO_SIM_anti_2 | 162 | 167 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 142 | 147 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 162 | 167 | PF11976 | 0.254 |
LIG_SUMO_SIM_par_1 | 230 | 235 | PF11976 | 0.426 |
LIG_SUMO_SIM_par_1 | 47 | 56 | PF11976 | 0.459 |
LIG_TRAF2_2 | 413 | 418 | PF00917 | 0.430 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.369 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.410 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.482 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.411 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.384 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.365 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.340 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.450 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.484 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.501 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.406 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.511 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.450 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.465 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.406 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.413 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.430 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.343 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.472 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.486 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.665 |
MOD_GlcNHglycan | 132 | 136 | PF01048 | 0.623 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.657 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.565 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.612 |
MOD_GlcNHglycan | 265 | 269 | PF01048 | 0.676 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.567 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.593 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.637 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.757 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.630 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.715 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.683 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.607 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.571 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.435 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.361 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.405 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.599 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.465 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.410 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.460 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.424 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.411 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.366 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.527 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.415 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.332 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.508 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.469 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.475 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.451 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.480 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.396 |
MOD_N-GLC_1 | 140 | 145 | PF02516 | 0.664 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.559 |
MOD_N-GLC_2 | 438 | 440 | PF02516 | 0.690 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.488 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.417 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.465 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.432 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.433 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.363 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.319 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.434 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.407 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.397 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.346 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.427 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.375 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.422 |
MOD_PIKK_1 | 360 | 366 | PF00454 | 0.440 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.472 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.368 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.506 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.532 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.447 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.484 |
MOD_Plk_1 | 184 | 190 | PF00069 | 0.365 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.395 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.429 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.501 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.309 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.466 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.486 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.359 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.382 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.484 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.354 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.382 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.493 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.393 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.380 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.373 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.400 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.555 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.366 |
TRG_NES_CRM1_1 | 128 | 139 | PF08389 | 0.450 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P251 | Leptomonas seymouri | 23% | 100% |
A0A381M9M8 | Leishmania infantum | 92% | 100% |
A0A3S5H581 | Leishmania donovani | 91% | 100% |
A0A3S5H583 | Leishmania donovani | 91% | 100% |
A0A451EJW1 | Leishmania donovani | 91% | 100% |
A0A451EJW4 | Leishmania donovani | 91% | 100% |
A0A451EJW6 | Leishmania donovani | 23% | 75% |
A4H3T7 | Leishmania braziliensis | 77% | 100% |
A4H3T8 | Leishmania braziliensis | 68% | 93% |
A4H3T9 | Leishmania braziliensis | 69% | 100% |
A4H3U0 | Leishmania braziliensis | 67% | 100% |
A4H3U1 | Leishmania braziliensis | 67% | 100% |
A4HS14 | Leishmania infantum | 23% | 75% |
E9AJZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 87% |
E9AK01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 75% |
Q9N852 | Leishmania major | 100% | 100% |
Q9N856 | Leishmania major | 100% | 100% |
Q9XZX9 | Leishmania major | 23% | 75% |