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: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A0A3Q8IET3
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 18 |
GO:0009987 | cellular process | 1 | 18 |
GO:0006458 | 'de novo' protein folding | 3 | 2 |
GO:0006950 | response to stress | 2 | 7 |
GO:0009266 | response to temperature stimulus | 3 | 7 |
GO:0009408 | response to heat | 3 | 7 |
GO:0009628 | response to abiotic stimulus | 2 | 7 |
GO:0042026 | protein refolding | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 7 |
GO:0051084 | 'de novo' post-translational protein folding | 4 | 2 |
GO:0051085 | chaperone cofactor-dependent protein refolding | 4 | 2 |
GO:0061077 | chaperone-mediated protein folding | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 18 |
GO:0005515 | protein binding | 2 | 18 |
GO:0031072 | heat shock protein binding | 3 | 18 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043169 | cation binding | 3 | 16 |
GO:0046872 | metal ion binding | 4 | 16 |
GO:0051082 | unfolded protein binding | 3 | 18 |
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 109 | 113 | PF00656 | 0.564 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.397 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.738 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.536 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.558 |
DOC_CKS1_1 | 281 | 286 | PF01111 | 0.474 |
DOC_CYCLIN_yClb1_LxF_4 | 62 | 67 | PF00134 | 0.382 |
DOC_CYCLIN_yCln2_LP_2 | 397 | 403 | PF00134 | 0.363 |
DOC_MAPK_DCC_7 | 428 | 437 | PF00069 | 0.282 |
DOC_MAPK_gen_1 | 474 | 481 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 428 | 437 | PF00069 | 0.282 |
DOC_PP1_RVXF_1 | 3 | 10 | PF00149 | 0.565 |
DOC_PP1_RVXF_1 | 62 | 68 | PF00149 | 0.544 |
DOC_PP2B_LxvP_1 | 397 | 400 | PF13499 | 0.360 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.322 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.614 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.473 |
LIG_14-3-3_CanoR_1 | 106 | 114 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 14 | 22 | PF00244 | 0.794 |
LIG_14-3-3_CanoR_1 | 248 | 252 | PF00244 | 0.285 |
LIG_14-3-3_CanoR_1 | 446 | 454 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 501 | 506 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 77 | 87 | PF00244 | 0.496 |
LIG_BIR_III_4 | 233 | 237 | PF00653 | 0.508 |
LIG_BRCT_BRCA1_1 | 501 | 505 | PF00533 | 0.436 |
LIG_CSL_BTD_1 | 33 | 36 | PF09270 | 0.565 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.396 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.487 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.335 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.442 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.570 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.709 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.643 |
LIG_HCF-1_HBM_1 | 379 | 382 | PF13415 | 0.282 |
LIG_LIR_Apic_2 | 436 | 441 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 112 | 122 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 456 | 466 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 59 | 68 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 112 | 117 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 456 | 462 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.437 |
LIG_OCRL_FandH_1 | 352 | 364 | PF00620 | 0.422 |
LIG_PTB_Apo_2 | 347 | 354 | PF02174 | 0.437 |
LIG_SH2_CRK | 114 | 118 | PF00017 | 0.383 |
LIG_SH2_CRK | 459 | 463 | PF00017 | 0.389 |
LIG_SH2_CRK | 62 | 66 | PF00017 | 0.495 |
LIG_SH2_SRC | 160 | 163 | PF00017 | 0.685 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 538 | 542 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.410 |
LIG_SH3_2 | 319 | 324 | PF14604 | 0.556 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.569 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.510 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.393 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.334 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.305 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.416 |
LIG_SUMO_SIM_anti_2 | 402 | 407 | PF11976 | 0.393 |
LIG_SUMO_SIM_par_1 | 373 | 379 | PF11976 | 0.335 |
LIG_TYR_ITIM | 457 | 462 | PF00017 | 0.384 |
MOD_CDC14_SPxK_1 | 386 | 389 | PF00782 | 0.282 |
MOD_CDK_SPK_2 | 280 | 285 | PF00069 | 0.322 |
MOD_CDK_SPxK_1 | 280 | 286 | PF00069 | 0.322 |
MOD_CDK_SPxK_1 | 383 | 389 | PF00069 | 0.282 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.755 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.611 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.713 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.634 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.587 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.555 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.479 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.586 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.446 |
MOD_CMANNOS | 34 | 37 | PF00535 | 0.697 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.676 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.632 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.665 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.731 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.656 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.360 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.326 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.321 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.394 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.509 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.482 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.423 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.758 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.573 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.664 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.682 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.720 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.609 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.319 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.415 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.316 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.398 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.372 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.558 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.767 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.635 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.574 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.480 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.321 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.393 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.292 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.443 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.402 |
MOD_NEK2_2 | 417 | 422 | PF00069 | 0.282 |
MOD_NEK2_2 | 57 | 62 | PF00069 | 0.593 |
MOD_PIKK_1 | 507 | 513 | PF00454 | 0.732 |
MOD_PKA_1 | 105 | 111 | PF00069 | 0.414 |
MOD_PKA_1 | 14 | 20 | PF00069 | 0.589 |
MOD_PKA_1 | 77 | 83 | PF00069 | 0.443 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.414 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.754 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.703 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.287 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.369 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.671 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.356 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.688 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.481 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.709 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.357 |
MOD_Plk_1 | 251 | 257 | PF00069 | 0.235 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.415 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.647 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.316 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.366 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.492 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.322 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.473 |
MOD_SUMO_rev_2 | 100 | 107 | PF00179 | 0.530 |
MOD_SUMO_rev_2 | 108 | 113 | PF00179 | 0.483 |
MOD_SUMO_rev_2 | 92 | 97 | PF00179 | 0.525 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.474 |
TRG_ER_diArg_1 | 353 | 356 | PF00400 | 0.340 |
TRG_ER_diArg_1 | 76 | 78 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 88 | 90 | PF00400 | 0.478 |
TRG_NES_CRM1_1 | 242 | 252 | PF08389 | 0.422 |
TRG_Pf-PMV_PEXEL_1 | 105 | 109 | PF00026 | 0.537 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZS2 | Leptomonas seymouri | 62% | 100% |
A0A0S4J3B2 | Bodo saltans | 33% | 100% |
A0A1X0NLD4 | Trypanosomatidae | 26% | 100% |
A0A1X0NWP1 | Trypanosomatidae | 45% | 100% |
A0A3R7KX88 | Trypanosoma rangeli | 43% | 100% |
A0A3S7WNT6 | Leishmania donovani | 26% | 100% |
A0A422N924 | Trypanosoma rangeli | 27% | 100% |
A4HS91 | Leishmania infantum | 26% | 100% |
A4HYQ6 | Leishmania infantum | 100% | 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 | 85% | 100% |
E9AK75 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 98% |
E9AUJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
O97016 | Leishmania major | 26% | 100% |
Q4QCY5 | Leishmania major | 95% | 100% |