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: 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: A4H5X1
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 | 76 | 80 | PF00656 | 0.288 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.513 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.272 |
CLV_PCSK_PC1ET2_1 | 204 | 206 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 270 | 272 | PF00082 | 0.795 |
CLV_PCSK_PC1ET2_1 | 382 | 384 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 60 | 62 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.652 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.548 |
DEG_SPOP_SBC_1 | 118 | 122 | PF00917 | 0.485 |
DEG_SPOP_SBC_1 | 386 | 390 | PF00917 | 0.494 |
DEG_SPOP_SBC_1 | 78 | 82 | PF00917 | 0.422 |
DOC_CYCLIN_RxL_1 | 99 | 109 | PF00134 | 0.533 |
DOC_MAPK_gen_1 | 41 | 49 | PF00069 | 0.454 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.349 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.651 |
LIG_14-3-3_CanoR_1 | 110 | 118 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 163 | 173 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 205 | 213 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 251 | 258 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 357 | 367 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 84 | 92 | PF00244 | 0.404 |
LIG_APCC_ABBA_1 | 221 | 226 | PF00400 | 0.389 |
LIG_BRCT_BRCA1_1 | 228 | 232 | PF00533 | 0.391 |
LIG_EH_1 | 312 | 316 | PF12763 | 0.592 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.455 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.443 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.421 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.314 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.328 |
LIG_LIR_Apic_2 | 323 | 328 | PF02991 | 0.622 |
LIG_LIR_Gen_1 | 229 | 237 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 293 | 303 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 229 | 233 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.761 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.524 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.741 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.271 |
LIG_SH2_CRK | 92 | 96 | PF00017 | 0.271 |
LIG_SH2_NCK_1 | 325 | 329 | PF00017 | 0.602 |
LIG_SH2_NCK_1 | 384 | 388 | PF00017 | 0.502 |
LIG_SH2_SRC | 224 | 227 | PF00017 | 0.406 |
LIG_SH2_SRC | 304 | 307 | PF00017 | 0.657 |
LIG_SH2_STAP1 | 145 | 149 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 304 | 308 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.461 |
LIG_SH3_CIN85_PxpxPR_1 | 184 | 189 | PF14604 | 0.515 |
LIG_TRAF2_1 | 307 | 310 | PF00917 | 0.616 |
MOD_CDK_SPxxK_3 | 180 | 187 | PF00069 | 0.510 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.669 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.573 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.519 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.556 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.404 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.404 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.566 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.593 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.616 |
MOD_Cter_Amidation | 202 | 205 | PF01082 | 0.630 |
MOD_Cter_Amidation | 409 | 412 | PF01082 | 0.513 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.584 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.773 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.584 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.540 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.640 |
MOD_GlcNHglycan | 305 | 309 | PF01048 | 0.614 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.557 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.722 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.729 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.767 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.356 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.362 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.505 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.635 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.581 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.520 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.727 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.697 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.670 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.335 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.358 |
MOD_LATS_1 | 275 | 281 | PF00433 | 0.492 |
MOD_LATS_1 | 401 | 407 | PF00433 | 0.506 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.666 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.559 |
MOD_N-GLC_1 | 359 | 364 | PF02516 | 0.711 |
MOD_N-GLC_1 | 74 | 79 | PF02516 | 0.360 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.708 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.616 |
MOD_NEK2_2 | 91 | 96 | PF00069 | 0.349 |
MOD_PKA_1 | 204 | 210 | PF00069 | 0.509 |
MOD_PKA_1 | 363 | 369 | PF00069 | 0.756 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.497 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.562 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.689 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.457 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.484 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.439 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.404 |
MOD_PKB_1 | 187 | 195 | PF00069 | 0.662 |
MOD_Plk_2-3 | 226 | 232 | PF00069 | 0.396 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.578 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.491 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.630 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.658 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.539 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.652 |
TRG_DiLeu_BaLyEn_6 | 139 | 144 | PF01217 | 0.374 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.659 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.319 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.577 |
TRG_NLS_Bipartite_1 | 260 | 274 | PF00514 | 0.568 |
TRG_NLS_Bipartite_1 | 41 | 63 | PF00514 | 0.335 |
TRG_NLS_MonoExtC_3 | 58 | 64 | PF00514 | 0.314 |
TRG_Pf-PMV_PEXEL_1 | 103 | 107 | PF00026 | 0.652 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I106 | Leptomonas seymouri | 57% | 98% |
A0A1X0NII8 | Trypanosomatidae | 41% | 100% |
A0A3Q8IC04 | Leishmania donovani | 78% | 100% |
A0A3R7KNF9 | Trypanosoma rangeli | 43% | 100% |
A4HU66 | Leishmania infantum | 78% | 100% |
D0A9P8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AMZ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4QHN1 | Leishmania major | 81% | 100% |
V5BMJ5 | Trypanosoma cruzi | 40% | 100% |