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: 1, no: 20 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: E9AIB2
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 22 |
GO:0009987 | cellular process | 1 | 22 |
GO:0006950 | response to stress | 2 | 10 |
GO:0009266 | response to temperature stimulus | 3 | 10 |
GO:0009408 | response to heat | 3 | 10 |
GO:0009628 | response to abiotic stimulus | 2 | 10 |
GO:0050896 | response to stimulus | 1 | 10 |
GO:0006458 | 'de novo' protein folding | 3 | 2 |
GO:0042026 | protein refolding | 3 | 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 | 22 |
GO:0005515 | protein binding | 2 | 22 |
GO:0031072 | heat shock protein binding | 3 | 22 |
GO:0043167 | ion binding | 2 | 21 |
GO:0043169 | cation binding | 3 | 20 |
GO:0046872 | metal ion binding | 4 | 20 |
GO:0051082 | unfolded protein binding | 3 | 22 |
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0030544 | Hsp70 protein binding | 4 | 1 |
GO:0051087 | protein-folding chaperone binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.314 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.220 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.457 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 71 | 73 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.471 |
DEG_COP1_1 | 159 | 167 | PF00400 | 0.420 |
DOC_CKS1_1 | 247 | 252 | PF01111 | 0.393 |
DOC_CKS1_1 | 478 | 483 | PF01111 | 0.478 |
DOC_CYCLIN_yCln2_LP_2 | 363 | 369 | PF00134 | 0.327 |
DOC_PP1_RVXF_1 | 28 | 34 | PF00149 | 0.481 |
DOC_PP2B_LxvP_1 | 363 | 366 | PF13499 | 0.291 |
DOC_PP2B_LxvP_1 | 465 | 468 | PF13499 | 0.444 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.263 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.567 |
DOC_USP7_UBL2_3 | 501 | 505 | PF12436 | 0.432 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.579 |
LIG_14-3-3_CanoR_1 | 157 | 165 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 214 | 218 | PF00244 | 0.213 |
LIG_14-3-3_CanoR_1 | 412 | 416 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 43 | 53 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 89 | 97 | PF00244 | 0.412 |
LIG_BIR_III_4 | 199 | 203 | PF00653 | 0.419 |
LIG_BIR_III_4 | 402 | 406 | PF00653 | 0.149 |
LIG_EH1_1 | 424 | 432 | PF00400 | 0.218 |
LIG_EVH1_2 | 467 | 471 | PF00568 | 0.451 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.320 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.427 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.267 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.353 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.714 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.720 |
LIG_LIR_Apic_2 | 402 | 407 | PF02991 | 0.193 |
LIG_LIR_Gen_1 | 26 | 34 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 78 | 88 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 78 | 83 | PF02991 | 0.388 |
LIG_PTB_Apo_2 | 313 | 320 | PF02174 | 0.381 |
LIG_SH2_CRK | 28 | 32 | PF00017 | 0.416 |
LIG_SH2_CRK | 425 | 429 | PF00017 | 0.334 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.354 |
LIG_SH2_SRC | 126 | 129 | PF00017 | 0.673 |
LIG_SH2_STAP1 | 92 | 96 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.673 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.472 |
LIG_SH3_2 | 285 | 290 | PF14604 | 0.509 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.514 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.470 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.151 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.259 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.225 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.353 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.474 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.354 |
LIG_SUMO_SIM_anti_2 | 225 | 230 | PF11976 | 0.164 |
LIG_SUMO_SIM_anti_2 | 368 | 373 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 339 | 345 | PF11976 | 0.310 |
LIG_TYR_ITIM | 423 | 428 | PF00017 | 0.331 |
MOD_CDK_SPK_2 | 246 | 251 | PF00069 | 0.220 |
MOD_CDK_SPxK_1 | 246 | 252 | PF00069 | 0.220 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.549 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.536 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.598 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.563 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.599 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.492 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.567 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.385 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.579 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.577 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.576 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.545 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.556 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.290 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.221 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.328 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.439 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.743 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.475 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.626 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.634 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.533 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.223 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.294 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.381 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.489 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.509 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.747 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.482 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.531 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.549 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.518 |
MOD_N-GLC_1 | 204 | 209 | PF02516 | 0.413 |
MOD_N-GLC_1 | 90 | 95 | PF02516 | 0.453 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.247 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.300 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.382 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.367 |
MOD_NEK2_2 | 23 | 28 | PF00069 | 0.521 |
MOD_NEK2_2 | 258 | 263 | PF00069 | 0.409 |
MOD_PKA_1 | 43 | 49 | PF00069 | 0.377 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.628 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.455 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.214 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.304 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.288 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.644 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.439 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.662 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.682 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.274 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.240 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.509 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.426 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.381 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.296 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.220 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.578 |
MOD_SUMO_rev_2 | 58 | 63 | PF00179 | 0.468 |
MOD_SUMO_rev_2 | 66 | 73 | PF00179 | 0.421 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.412 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.530 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZS2 | Leptomonas seymouri | 62% | 96% |
A0A0N1I257 | Leptomonas seymouri | 27% | 100% |
A0A0S4J3B2 | Bodo saltans | 34% | 100% |
A0A1X0NLD4 | Trypanosomatidae | 27% | 100% |
A0A1X0NWP1 | Trypanosomatidae | 45% | 100% |
A0A3Q8IET3 | Leishmania donovani | 85% | 94% |
A0A3R7KX88 | Trypanosoma rangeli | 43% | 100% |
A0A3S7WNT6 | Leishmania donovani | 27% | 100% |
A0A422N924 | Trypanosoma rangeli | 27% | 100% |
A4H3Y7 | Leishmania braziliensis | 28% | 100% |
A4HS91 | Leishmania infantum | 27% | 100% |
A4HYQ6 | Leishmania infantum | 85% | 94% |
C9ZI72 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
C9ZY84 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AK75 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AUJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 94% |
O97016 | Leishmania major | 28% | 100% |
Q493S6 | Blochmannia pennsylvanicus (strain BPEN) | 25% | 100% |
Q4Q9Y3 | Leishmania major | 26% | 100% |
Q4QCY5 | Leishmania major | 84% | 100% |
V5AY81 | Trypanosoma cruzi | 27% | 100% |