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)
Proteases, peptidase M8
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: 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: A0A381M9M8
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 | 359 | 363 | PF00656 | 0.596 |
CLV_C14_Caspase3-7 | 37 | 41 | PF00656 | 0.340 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.586 |
DOC_MAPK_FxFP_2 | 282 | 285 | PF00069 | 0.586 |
DOC_PP4_FxxP_1 | 282 | 285 | PF00568 | 0.615 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.479 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.454 |
LIG_14-3-3_CanoR_1 | 116 | 126 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 220 | 228 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 439 | 447 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 490 | 496 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 88 | 92 | PF00244 | 0.468 |
LIG_BRCT_BRCA1_1 | 236 | 240 | PF00533 | 0.631 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.570 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.644 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.496 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.590 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.450 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.567 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.301 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.573 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.450 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.323 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.563 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.633 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.419 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.628 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.547 |
LIG_LIR_Gen_1 | 44 | 52 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 471 | 480 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 132 | 136 | PF02991 | 0.638 |
LIG_LIR_Nem_3 | 304 | 310 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 471 | 477 | PF02991 | 0.533 |
LIG_PDZ_Class_2 | 523 | 528 | PF00595 | 0.651 |
LIG_SH2_CRK | 474 | 478 | PF00017 | 0.529 |
LIG_SH2_SRC | 269 | 272 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 46 | 50 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.547 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.665 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.569 |
LIG_SUMO_SIM_anti_2 | 162 | 167 | PF11976 | 0.616 |
LIG_SUMO_SIM_par_1 | 101 | 106 | PF11976 | 0.285 |
LIG_SUMO_SIM_par_1 | 142 | 147 | PF11976 | 0.622 |
LIG_SUMO_SIM_par_1 | 162 | 167 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 193 | 199 | PF11976 | 0.529 |
LIG_SUMO_SIM_par_1 | 230 | 235 | PF11976 | 0.626 |
LIG_SUMO_SIM_par_1 | 47 | 56 | PF11976 | 0.434 |
LIG_TRAF2_2 | 413 | 418 | PF00917 | 0.584 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.356 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.584 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.534 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.508 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.517 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.652 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.611 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.568 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.558 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.612 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.600 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.486 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.668 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.341 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.376 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.391 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.609 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.621 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.611 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.453 |
MOD_GlcNHglycan | 132 | 136 | PF01048 | 0.435 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.438 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.366 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.453 |
MOD_GlcNHglycan | 265 | 269 | PF01048 | 0.344 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.266 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.344 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.411 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.459 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.377 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.460 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.623 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.583 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.552 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.632 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.546 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.641 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.553 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.646 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.621 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.650 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.592 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.538 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.669 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.602 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.659 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.638 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.610 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.526 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.278 |
MOD_N-GLC_1 | 140 | 145 | PF02516 | 0.430 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.342 |
MOD_N-GLC_2 | 438 | 440 | PF02516 | 0.381 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.620 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.571 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.618 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.615 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.532 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.522 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.577 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.348 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.328 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.412 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.555 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.603 |
MOD_PIKK_1 | 360 | 366 | PF00454 | 0.585 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.438 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.552 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.656 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.502 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.425 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.649 |
MOD_Plk_1 | 184 | 190 | PF00069 | 0.551 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.589 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.636 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.464 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.358 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.636 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.548 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.554 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.630 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.608 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.612 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.660 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.630 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.363 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.343 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.452 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.533 |
TRG_NES_CRM1_1 | 128 | 139 | PF08389 | 0.618 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H581 | Leishmania donovani | 97% | 100% |
A0A3S5H583 | Leishmania donovani | 98% | 100% |
A0A451EJW1 | Leishmania donovani | 97% | 100% |
A0A451EJW4 | Leishmania donovani | 98% | 100% |
A0A451EJW6 | Leishmania donovani | 23% | 74% |
A4H3T7 | Leishmania braziliensis | 76% | 100% |
A4H3T8 | Leishmania braziliensis | 69% | 100% |
A4H3T9 | Leishmania braziliensis | 69% | 100% |
A4H3U0 | Leishmania braziliensis | 67% | 100% |
A4H3U1 | Leishmania braziliensis | 67% | 100% |
A4HS14 | Leishmania infantum | 22% | 74% |
E9AJZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E9AK01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 74% |
Q9N852 | Leishmania major | 92% | 100% |
Q9N853 | Leishmania major | 92% | 100% |
Q9N856 | Leishmania major | 92% | 100% |
Q9XZX9 | Leishmania major | 24% | 74% |