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. | no | yes: 0 |
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: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005814 | centriole | 5 | 3 |
GO:0005874 | microtubule | 6 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043228 | non-membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 3 |
GO:0099080 | supramolecular complex | 2 | 3 |
GO:0099081 | supramolecular polymer | 3 | 3 |
GO:0099512 | supramolecular fiber | 4 | 3 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4HCY4
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 3 |
GO:0016043 | cellular component organization | 3 | 3 |
GO:0030030 | cell projection organization | 4 | 3 |
GO:0071840 | cellular component organization or biogenesis | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 102 | 106 | PF00656 | 0.452 |
CLV_C14_Caspase3-7 | 299 | 303 | PF00656 | 0.499 |
CLV_C14_Caspase3-7 | 421 | 425 | PF00656 | 0.705 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.613 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 237 | 239 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 458 | 460 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 501 | 503 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 86 | 88 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.708 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.387 |
DOC_MAPK_gen_1 | 101 | 110 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 214 | 224 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 237 | 245 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 482 | 493 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 501 | 507 | PF00069 | 0.312 |
DOC_MAPK_gen_1 | 86 | 93 | PF00069 | 0.493 |
DOC_PP2B_LxvP_1 | 265 | 268 | PF13499 | 0.571 |
DOC_SPAK_OSR1_1 | 502 | 506 | PF12202 | 0.451 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.546 |
DOC_USP7_UBL2_3 | 463 | 467 | PF12436 | 0.492 |
DOC_USP7_UBL2_3 | 482 | 486 | PF12436 | 0.326 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.503 |
LIG_14-3-3_CanoR_1 | 253 | 261 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 362 | 366 | PF00244 | 0.499 |
LIG_Actin_WH2_2 | 274 | 291 | PF00022 | 0.455 |
LIG_BIR_III_4 | 319 | 323 | PF00653 | 0.525 |
LIG_FAT_LD_1 | 507 | 515 | PF03623 | 0.377 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.465 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.446 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.463 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.490 |
LIG_LIR_Gen_1 | 33 | 41 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.444 |
LIG_NRBOX | 506 | 512 | PF00104 | 0.376 |
LIG_PCNA_yPIPBox_3 | 501 | 511 | PF02747 | 0.449 |
LIG_SH2_STAP1 | 442 | 446 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.390 |
LIG_SH3_4 | 326 | 333 | PF00018 | 0.669 |
LIG_SUMO_SIM_anti_2 | 512 | 518 | PF11976 | 0.300 |
LIG_SUMO_SIM_par_1 | 412 | 418 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 445 | 451 | PF11976 | 0.480 |
LIG_TRAF2_1 | 239 | 242 | PF00917 | 0.607 |
LIG_UBA3_1 | 414 | 422 | PF00899 | 0.459 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.414 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.340 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.643 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.599 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.459 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.600 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.457 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.488 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.523 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.477 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.568 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.447 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.735 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.671 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.511 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.492 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.715 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.507 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.475 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.477 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.409 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.420 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.518 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.439 |
MOD_LATS_1 | 192 | 198 | PF00433 | 0.577 |
MOD_N-GLC_1 | 125 | 130 | PF02516 | 0.431 |
MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.537 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.530 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.469 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.626 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.450 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.547 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.573 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.525 |
MOD_PIKK_1 | 409 | 415 | PF00454 | 0.643 |
MOD_PIKK_1 | 458 | 464 | PF00454 | 0.337 |
MOD_PIKK_1 | 495 | 501 | PF00454 | 0.455 |
MOD_PK_1 | 140 | 146 | PF00069 | 0.503 |
MOD_PK_1 | 194 | 200 | PF00069 | 0.457 |
MOD_PK_1 | 369 | 375 | PF00069 | 0.489 |
MOD_PKA_1 | 163 | 169 | PF00069 | 0.485 |
MOD_PKA_1 | 194 | 200 | PF00069 | 0.457 |
MOD_PKA_1 | 458 | 464 | PF00069 | 0.337 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.525 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.356 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.450 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.501 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.389 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.424 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.569 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.487 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.551 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.511 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.386 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.466 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.533 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.458 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.496 |
MOD_SUMO_rev_2 | 16 | 25 | PF00179 | 0.532 |
MOD_SUMO_rev_2 | 241 | 250 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 35 | 44 | PF00179 | 0.306 |
MOD_SUMO_rev_2 | 378 | 386 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 461 | 468 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 479 | 484 | PF00179 | 0.362 |
MOD_SUMO_rev_2 | 490 | 498 | PF00179 | 0.291 |
TRG_DiLeu_BaEn_1 | 487 | 492 | PF01217 | 0.478 |
TRG_DiLeu_BaEn_4 | 401 | 407 | PF01217 | 0.481 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 274 | 277 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 288 | 290 | PF00400 | 0.457 |
TRG_NES_CRM1_1 | 178 | 193 | PF08389 | 0.332 |
TRG_Pf-PMV_PEXEL_1 | 279 | 284 | PF00026 | 0.343 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NWV0 | Trypanosomatidae | 28% | 68% |
A0A3Q8IB33 | Leishmania donovani | 80% | 83% |
A0A422NPG5 | Trypanosoma rangeli | 27% | 69% |
A4I0G9 | Leishmania infantum | 80% | 83% |
E9AWD1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 83% |
Q4QB41 | Leishmania major | 80% | 100% |
V5BB81 | Trypanosoma cruzi | 28% | 69% |