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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 20 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: Q4QCY5
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 21 |
GO:0006458 | 'de novo' protein folding | 3 | 3 |
GO:0009987 | cellular process | 1 | 21 |
GO:0042026 | protein refolding | 3 | 3 |
GO:0051084 | 'de novo' post-translational protein folding | 4 | 3 |
GO:0051085 | chaperone cofactor-dependent protein refolding | 4 | 3 |
GO:0061077 | chaperone-mediated protein folding | 3 | 3 |
GO:0006950 | response to stress | 2 | 9 |
GO:0009266 | response to temperature stimulus | 3 | 9 |
GO:0009408 | response to heat | 3 | 9 |
GO:0009628 | response to abiotic stimulus | 2 | 9 |
GO:0050896 | response to stimulus | 1 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 21 |
GO:0005515 | protein binding | 2 | 21 |
GO:0031072 | heat shock protein binding | 3 | 21 |
GO:0043167 | ion binding | 2 | 20 |
GO:0043169 | cation binding | 3 | 19 |
GO:0046872 | metal ion binding | 4 | 19 |
GO:0051082 | unfolded protein binding | 3 | 21 |
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0030544 | Hsp70 protein binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.357 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.470 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.510 |
DOC_CKS1_1 | 281 | 286 | PF01111 | 0.428 |
DOC_CYCLIN_yClb1_LxF_4 | 62 | 67 | PF00134 | 0.337 |
DOC_CYCLIN_yCln2_LP_2 | 397 | 403 | PF00134 | 0.354 |
DOC_MAPK_DCC_7 | 428 | 437 | PF00069 | 0.235 |
DOC_MAPK_gen_1 | 474 | 481 | PF00069 | 0.364 |
DOC_MAPK_MEF2A_6 | 428 | 437 | PF00069 | 0.235 |
DOC_PP1_RVXF_1 | 3 | 10 | PF00149 | 0.510 |
DOC_PP1_RVXF_1 | 62 | 68 | PF00149 | 0.512 |
DOC_PP2B_LxvP_1 | 397 | 400 | PF13499 | 0.319 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.284 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.618 |
DOC_USP7_UBL2_3 | 535 | 539 | PF12436 | 0.432 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.376 |
LIG_14-3-3_CanoR_1 | 106 | 114 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 14 | 22 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 248 | 252 | PF00244 | 0.244 |
LIG_14-3-3_CanoR_1 | 446 | 454 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 501 | 506 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 77 | 87 | PF00244 | 0.438 |
LIG_BIR_III_4 | 233 | 237 | PF00653 | 0.440 |
LIG_CSL_BTD_1 | 33 | 36 | PF09270 | 0.502 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.364 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.442 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.298 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.278 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.379 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.316 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.737 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.470 |
LIG_HCF-1_HBM_1 | 379 | 382 | PF13415 | 0.235 |
LIG_LIR_Gen_1 | 456 | 466 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 59 | 68 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 456 | 462 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.411 |
LIG_OCRL_FandH_1 | 352 | 364 | PF00620 | 0.386 |
LIG_PTB_Apo_2 | 347 | 354 | PF02174 | 0.403 |
LIG_SH2_CRK | 459 | 463 | PF00017 | 0.327 |
LIG_SH2_CRK | 62 | 66 | PF00017 | 0.442 |
LIG_SH2_SRC | 160 | 163 | PF00017 | 0.700 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.700 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.372 |
LIG_SH3_2 | 319 | 324 | PF14604 | 0.525 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.512 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.491 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.319 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.274 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.249 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.376 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.429 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.379 |
LIG_SUMO_SIM_anti_2 | 402 | 407 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 373 | 379 | PF11976 | 0.294 |
LIG_TYR_ITIM | 457 | 462 | PF00017 | 0.323 |
MOD_CDC14_SPxK_1 | 386 | 389 | PF00782 | 0.235 |
MOD_CDK_SPK_2 | 280 | 285 | PF00069 | 0.268 |
MOD_CDK_SPxK_1 | 280 | 286 | PF00069 | 0.268 |
MOD_CDK_SPxK_1 | 383 | 389 | PF00069 | 0.235 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.690 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.585 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.627 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.590 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.589 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.497 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.553 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.413 |
MOD_CMANNOS | 34 | 37 | PF00535 | 0.646 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.646 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.619 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.604 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.622 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.606 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.572 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.310 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.297 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.292 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.358 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.555 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.463 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.535 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.730 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.535 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.642 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.632 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.620 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.557 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.248 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.372 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.337 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.411 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.421 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.323 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.724 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.574 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.516 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.274 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.345 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.256 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.477 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.427 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.393 |
MOD_NEK2_2 | 18 | 23 | PF00069 | 0.501 |
MOD_NEK2_2 | 417 | 422 | PF00069 | 0.235 |
MOD_NEK2_2 | 57 | 62 | PF00069 | 0.552 |
MOD_PIKK_1 | 507 | 513 | PF00454 | 0.720 |
MOD_PKA_1 | 105 | 111 | PF00069 | 0.386 |
MOD_PKA_1 | 14 | 20 | PF00069 | 0.536 |
MOD_PKA_1 | 77 | 83 | PF00069 | 0.387 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.366 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.722 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.662 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.237 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.328 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.678 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.318 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.666 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.438 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.309 |
MOD_Plk_1 | 251 | 257 | PF00069 | 0.270 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.413 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.579 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.291 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.324 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.454 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.291 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.376 |
MOD_SUMO_rev_2 | 100 | 107 | PF00179 | 0.446 |
MOD_SUMO_rev_2 | 108 | 113 | PF00179 | 0.411 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.444 |
TRG_ER_diArg_1 | 353 | 356 | PF00400 | 0.299 |
TRG_ER_diArg_1 | 76 | 78 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 88 | 90 | PF00400 | 0.435 |
TRG_NES_CRM1_1 | 242 | 252 | PF08389 | 0.386 |
TRG_Pf-PMV_PEXEL_1 | 105 | 109 | PF00026 | 0.493 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZS2 | Leptomonas seymouri | 61% | 100% |
A0A0S4J3B2 | Bodo saltans | 33% | 100% |
A0A1X0NLD4 | Trypanosomatidae | 27% | 100% |
A0A1X0NWP1 | Trypanosomatidae | 45% | 100% |
A0A3Q8IET3 | Leishmania donovani | 95% | 100% |
A0A3R7KX88 | Trypanosoma rangeli | 40% | 100% |
A0A3S7WNT6 | Leishmania donovani | 26% | 100% |
A0A422N924 | Trypanosoma rangeli | 26% | 100% |
A4H3Y7 | Leishmania braziliensis | 26% | 100% |
A4H886 | Leishmania braziliensis | 25% | 100% |
A4HS91 | Leishmania infantum | 26% | 100% |
A4HYQ6 | Leishmania infantum | 95% | 100% |
C9ZI72 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
C9ZY84 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9AIB2 | Leishmania braziliensis | 84% | 100% |
E9AK75 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AUJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
O97016 | Leishmania major | 26% | 100% |
Q8DKR7 | Thermosynechococcus vestitus (strain NIES-2133 / IAM M-273 / BP-1) | 25% | 100% |
V5AY81 | Trypanosoma cruzi | 26% | 100% |