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. | yes | yes: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IC04
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 1 |
GO:0006458 | 'de novo' protein folding | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0042026 | protein refolding | 3 | 1 |
GO:0051084 | 'de novo' post-translational protein folding | 4 | 1 |
GO:0051085 | chaperone cofactor-dependent protein refolding | 4 | 1 |
GO:0061077 | chaperone-mediated protein folding | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0051082 | unfolded protein binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 127 | 131 | PF00656 | 0.713 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.549 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.279 |
CLV_PCSK_PC1ET2_1 | 270 | 272 | PF00082 | 0.580 |
CLV_PCSK_PC1ET2_1 | 60 | 62 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.659 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.620 |
DEG_SPOP_SBC_1 | 78 | 82 | PF00917 | 0.439 |
DOC_CYCLIN_RxL_1 | 99 | 109 | PF00134 | 0.565 |
DOC_MAPK_gen_1 | 41 | 49 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 5 | 11 | PF00069 | 0.554 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.357 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.661 |
LIG_14-3-3_CanoR_1 | 14 | 20 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 251 | 258 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 357 | 365 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 84 | 92 | PF00244 | 0.420 |
LIG_AP2alpha_2 | 313 | 315 | PF02296 | 0.583 |
LIG_APCC_ABBA_1 | 221 | 226 | PF00400 | 0.398 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.536 |
LIG_BRCT_BRCA1_1 | 228 | 232 | PF00533 | 0.399 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.472 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.425 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.322 |
LIG_LIR_Apic_2 | 175 | 180 | PF02991 | 0.665 |
LIG_LIR_Apic_2 | 322 | 328 | PF02991 | 0.638 |
LIG_LIR_Gen_1 | 229 | 237 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 293 | 303 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 229 | 233 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 313 | 318 | PF02991 | 0.732 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.769 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.750 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.279 |
LIG_SH2_CRK | 92 | 96 | PF00017 | 0.279 |
LIG_SH2_NCK_1 | 325 | 329 | PF00017 | 0.628 |
LIG_SH2_SRC | 224 | 227 | PF00017 | 0.416 |
LIG_SH2_SRC | 329 | 332 | PF00017 | 0.657 |
LIG_SH2_STAP1 | 145 | 149 | PF00017 | 0.429 |
LIG_SH2_STAT3 | 126 | 129 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.618 |
LIG_TRAF2_1 | 307 | 310 | PF00917 | 0.644 |
LIG_WW_3 | 178 | 182 | PF00397 | 0.692 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.598 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.615 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.756 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.606 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.551 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.628 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.410 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.592 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.624 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.643 |
MOD_Cter_Amidation | 101 | 104 | PF01082 | 0.477 |
MOD_Cter_Amidation | 202 | 205 | PF01082 | 0.652 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.586 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.538 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.783 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.696 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.572 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.650 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.605 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.761 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.671 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.357 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.398 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.614 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.593 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.591 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.598 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.745 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.635 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.355 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.397 |
MOD_N-GLC_1 | 112 | 117 | PF02516 | 0.616 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.779 |
MOD_N-GLC_1 | 359 | 364 | PF02516 | 0.745 |
MOD_N-GLC_1 | 74 | 79 | PF02516 | 0.369 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.677 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.615 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.545 |
MOD_NEK2_2 | 91 | 96 | PF00069 | 0.357 |
MOD_PKA_1 | 204 | 210 | PF00069 | 0.532 |
MOD_PKA_1 | 363 | 369 | PF00069 | 0.791 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.694 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.690 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.450 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.420 |
MOD_PKB_1 | 187 | 195 | PF00069 | 0.680 |
MOD_Plk_2-3 | 226 | 232 | PF00069 | 0.404 |
MOD_Plk_2-3 | 305 | 311 | PF00069 | 0.684 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.586 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.592 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.663 |
TRG_DiLeu_BaEn_2 | 156 | 162 | PF01217 | 0.433 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.678 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.279 |
TRG_ER_diArg_1 | 103 | 105 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 271 | 274 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 382 | 384 | PF00400 | 0.638 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.682 |
TRG_NLS_Bipartite_1 | 260 | 274 | PF00514 | 0.579 |
TRG_NLS_Bipartite_1 | 41 | 63 | PF00514 | 0.355 |
TRG_NLS_MonoExtC_3 | 58 | 64 | PF00514 | 0.322 |
TRG_Pf-PMV_PEXEL_1 | 103 | 107 | PF00026 | 0.658 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I106 | Leptomonas seymouri | 56% | 98% |
A0A1X0NII8 | Trypanosomatidae | 39% | 100% |
A0A3R7KNF9 | Trypanosoma rangeli | 41% | 100% |
A4H5X1 | Leishmania braziliensis | 78% | 100% |
A4HU66 | Leishmania infantum | 100% | 100% |
D0A9P8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AMZ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QHN1 | Leishmania major | 94% | 100% |
V5BMJ5 | Trypanosoma cruzi | 38% | 100% |