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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AUJ9
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 14 |
GO:0009987 | cellular process | 1 | 14 |
GO:0006458 | 'de novo' protein folding | 3 | 2 |
GO:0006950 | response to stress | 2 | 3 |
GO:0009266 | response to temperature stimulus | 3 | 3 |
GO:0009408 | response to heat | 3 | 3 |
GO:0009628 | response to abiotic stimulus | 2 | 3 |
GO:0042026 | protein refolding | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 3 |
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 | 14 |
GO:0005515 | protein binding | 2 | 14 |
GO:0031072 | heat shock protein binding | 3 | 14 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043169 | cation binding | 3 | 13 |
GO:0046872 | metal ion binding | 4 | 13 |
GO:0051082 | unfolded protein binding | 3 | 14 |
GO:0000166 | nucleotide binding | 3 | 3 |
GO:0005524 | ATP binding | 5 | 3 |
GO:0017076 | purine nucleotide binding | 4 | 3 |
GO:0030554 | adenyl nucleotide binding | 5 | 3 |
GO:0032553 | ribonucleotide binding | 3 | 3 |
GO:0032555 | purine ribonucleotide binding | 4 | 3 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 3 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 3 |
GO:0036094 | small molecule binding | 2 | 3 |
GO:0043168 | anion binding | 3 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 3 |
GO:0097367 | carbohydrate derivative binding | 2 | 3 |
GO:1901265 | nucleoside phosphate binding | 3 | 3 |
GO:1901363 | heterocyclic compound binding | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 108 | 112 | PF00656 | 0.384 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.246 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.370 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 104 | 106 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 475 | 479 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.571 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.540 |
DOC_CKS1_1 | 280 | 285 | PF01111 | 0.460 |
DOC_CKS1_1 | 511 | 516 | PF01111 | 0.510 |
DOC_CYCLIN_yClb1_LxF_4 | 61 | 66 | PF00134 | 0.368 |
DOC_CYCLIN_yCln2_LP_2 | 396 | 402 | PF00134 | 0.356 |
DOC_MAPK_DCC_7 | 427 | 436 | PF00069 | 0.269 |
DOC_MAPK_gen_1 | 473 | 480 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 427 | 436 | PF00069 | 0.269 |
DOC_PP1_RVXF_1 | 3 | 10 | PF00149 | 0.532 |
DOC_PP1_RVXF_1 | 61 | 67 | PF00149 | 0.512 |
DOC_PP2B_LxvP_1 | 396 | 399 | PF13499 | 0.322 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.311 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.613 |
DOC_USP7_UBL2_3 | 534 | 538 | PF12436 | 0.582 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.605 |
LIG_14-3-3_CanoR_1 | 105 | 113 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 14 | 23 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 247 | 251 | PF00244 | 0.275 |
LIG_14-3-3_CanoR_1 | 445 | 453 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 500 | 505 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 76 | 86 | PF00244 | 0.503 |
LIG_BIR_III_4 | 232 | 236 | PF00653 | 0.490 |
LIG_CSL_BTD_1 | 32 | 35 | PF09270 | 0.526 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.350 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.451 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.297 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.430 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.423 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.679 |
LIG_FHA_2 | 489 | 495 | PF00498 | 0.687 |
LIG_HCF-1_HBM_1 | 378 | 381 | PF13415 | 0.269 |
LIG_Integrin_RGD_1 | 466 | 468 | PF01839 | 0.469 |
LIG_LIR_Apic_2 | 435 | 440 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 111 | 121 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 58 | 67 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.434 |
LIG_OCRL_FandH_1 | 351 | 363 | PF00620 | 0.388 |
LIG_PTB_Apo_2 | 346 | 353 | PF02174 | 0.405 |
LIG_SH2_CRK | 113 | 117 | PF00017 | 0.359 |
LIG_SH2_CRK | 458 | 462 | PF00017 | 0.364 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.502 |
LIG_SH2_SRC | 159 | 162 | PF00017 | 0.698 |
LIG_SH2_STAP1 | 125 | 129 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.698 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.444 |
LIG_SH3_1 | 29 | 35 | PF00018 | 0.416 |
LIG_SH3_2 | 318 | 323 | PF14604 | 0.527 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.533 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.492 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.163 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.303 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.287 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.564 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.394 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.415 |
LIG_SUMO_SIM_anti_2 | 401 | 406 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 372 | 378 | PF11976 | 0.297 |
LIG_TYR_ITIM | 456 | 461 | PF00017 | 0.362 |
MOD_CDC14_SPxK_1 | 385 | 388 | PF00782 | 0.269 |
MOD_CDK_SPK_2 | 279 | 284 | PF00069 | 0.311 |
MOD_CDK_SPxK_1 | 279 | 285 | PF00069 | 0.311 |
MOD_CDK_SPxK_1 | 382 | 388 | PF00069 | 0.269 |
MOD_CDK_SPxxK_3 | 316 | 323 | PF00069 | 0.243 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.686 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.682 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.616 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.610 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.576 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.629 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.427 |
MOD_CMANNOS | 33 | 36 | PF00535 | 0.638 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.617 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.734 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.631 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.351 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.297 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.283 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.440 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.463 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.472 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.753 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.538 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.543 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.675 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.579 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.272 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.408 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.325 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.405 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.405 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.513 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.722 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.425 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.562 |
MOD_N-GLC_1 | 223 | 228 | PF02516 | 0.522 |
MOD_N-GLC_1 | 237 | 242 | PF02516 | 0.440 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.298 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.400 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.262 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.435 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.461 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.417 |
MOD_NEK2_2 | 17 | 22 | PF00069 | 0.482 |
MOD_NEK2_2 | 416 | 421 | PF00069 | 0.269 |
MOD_NEK2_2 | 56 | 61 | PF00069 | 0.549 |
MOD_OFUCOSY | 10 | 17 | PF10250 | 0.424 |
MOD_PIKK_1 | 506 | 512 | PF00454 | 0.731 |
MOD_PKA_1 | 104 | 110 | PF00069 | 0.576 |
MOD_PKA_1 | 76 | 82 | PF00069 | 0.430 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.398 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.667 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.667 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.278 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.331 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.318 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.648 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.441 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.671 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.309 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.301 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.405 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.629 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.278 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.475 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.464 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.311 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.225 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.446 |
MOD_ProDKin_1 | 510 | 516 | PF00069 | 0.605 |
MOD_SUMO_rev_2 | 107 | 112 | PF00179 | 0.484 |
MOD_SUMO_rev_2 | 91 | 96 | PF00179 | 0.511 |
MOD_SUMO_rev_2 | 99 | 106 | PF00179 | 0.479 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.499 |
TRG_ER_diArg_1 | 352 | 355 | PF00400 | 0.302 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.437 |
TRG_NES_CRM1_1 | 241 | 251 | PF08389 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 104 | 108 | PF00026 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZS2 | Leptomonas seymouri | 63% | 100% |
A0A0S4J3B2 | Bodo saltans | 34% | 100% |
A0A1X0NLD4 | Trypanosomatidae | 26% | 100% |
A0A1X0NWP1 | Trypanosomatidae | 45% | 100% |
A0A3Q8IET3 | Leishmania donovani | 93% | 100% |
A0A3R7KX88 | Trypanosoma rangeli | 40% | 100% |
A0A3S7WNT6 | Leishmania donovani | 26% | 100% |
A0A422N924 | Trypanosoma rangeli | 26% | 100% |
A4H3Y7 | Leishmania braziliensis | 27% | 100% |
A4HS91 | Leishmania infantum | 26% | 100% |
A4HYQ6 | Leishmania infantum | 93% | 100% |
A8GMF8 | Rickettsia akari (strain Hartford) | 24% | 100% |
B5YAR4 | Dictyoglomus thermophilum (strain ATCC 35947 / DSM 3960 / H-6-12) | 27% | 100% |
C9ZI72 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
C9ZY84 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AIB2 | Leishmania braziliensis | 86% | 100% |
E9AK75 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
O97016 | Leishmania major | 27% | 100% |
Q493S6 | Blochmannia pennsylvanicus (strain BPEN) | 22% | 100% |
Q4QCY5 | Leishmania major | 92% | 100% |
Q8DKR7 | Thermosynechococcus vestitus (strain NIES-2133 / IAM M-273 / BP-1) | 25% | 100% |
V5AY81 | Trypanosoma cruzi | 25% | 100% |