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: E9AMZ6
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_NRD_NRD_1 | 103 | 105 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.592 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.272 |
CLV_PCSK_PC1ET2_1 | 60 | 62 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.609 |
DEG_SPOP_SBC_1 | 78 | 82 | PF00917 | 0.422 |
DOC_CYCLIN_RxL_1 | 99 | 109 | PF00134 | 0.534 |
DOC_MAPK_gen_1 | 41 | 49 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 5 | 11 | PF00069 | 0.533 |
DOC_PP4_FxxP_1 | 168 | 171 | PF00568 | 0.497 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.792 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.349 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.661 |
LIG_14-3-3_CanoR_1 | 14 | 20 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 249 | 256 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 355 | 363 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 84 | 92 | PF00244 | 0.404 |
LIG_APCC_ABBA_1 | 219 | 224 | PF00400 | 0.390 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.515 |
LIG_BRCT_BRCA1_1 | 226 | 230 | PF00533 | 0.394 |
LIG_EH_1 | 310 | 314 | PF12763 | 0.598 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.463 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.419 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.314 |
LIG_LIR_Apic_2 | 166 | 171 | PF02991 | 0.661 |
LIG_LIR_Apic_2 | 173 | 178 | PF02991 | 0.665 |
LIG_LIR_Apic_2 | 321 | 326 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 227 | 235 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 291 | 301 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 227 | 231 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 331 | 336 | PF02991 | 0.773 |
LIG_Pex14_1 | 7 | 11 | PF04695 | 0.496 |
LIG_SH2_CRK | 323 | 327 | PF00017 | 0.751 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.271 |
LIG_SH2_CRK | 92 | 96 | PF00017 | 0.271 |
LIG_SH2_NCK_1 | 323 | 327 | PF00017 | 0.612 |
LIG_SH2_SRC | 222 | 225 | PF00017 | 0.410 |
LIG_SH2_STAP1 | 143 | 147 | PF00017 | 0.422 |
LIG_SH2_STAT3 | 124 | 127 | PF00017 | 0.615 |
LIG_TRAF2_1 | 125 | 128 | PF00917 | 0.456 |
LIG_TRAF2_1 | 305 | 308 | PF00917 | 0.620 |
LIG_WW_3 | 176 | 180 | PF00397 | 0.687 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.683 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.729 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.597 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.532 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.595 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.404 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.482 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.585 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.595 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.620 |
MOD_Cter_Amidation | 101 | 104 | PF01082 | 0.472 |
MOD_Cter_Amidation | 200 | 203 | PF01082 | 0.640 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.547 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.784 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.570 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.543 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.633 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.550 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.559 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.738 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.740 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.755 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.358 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.363 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.515 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.665 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.544 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.629 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.549 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.554 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.702 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.335 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.358 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.683 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.782 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.715 |
MOD_N-GLC_1 | 74 | 79 | PF02516 | 0.360 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.716 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.581 |
MOD_NEK2_2 | 91 | 96 | PF00069 | 0.349 |
MOD_PKA_1 | 202 | 208 | PF00069 | 0.524 |
MOD_PKA_1 | 361 | 367 | PF00069 | 0.768 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.690 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.444 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.404 |
MOD_PKB_1 | 185 | 193 | PF00069 | 0.665 |
MOD_Plk_2-3 | 224 | 230 | PF00069 | 0.399 |
MOD_Plk_2-3 | 303 | 309 | PF00069 | 0.676 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.446 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.541 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.661 |
MOD_SUMO_rev_2 | 189 | 198 | PF00179 | 0.501 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.668 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.578 |
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 | 103 | 105 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 150 | 152 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 268 | 271 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 380 | 382 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.569 |
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 | 0.656 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I106 | Leptomonas seymouri | 56% | 97% |
A0A1X0NII8 | Trypanosomatidae | 39% | 100% |
A0A3Q8IC04 | Leishmania donovani | 90% | 100% |
A0A3R7KNF9 | Trypanosoma rangeli | 39% | 100% |
A4H5X1 | Leishmania braziliensis | 78% | 100% |
A4HU66 | Leishmania infantum | 90% | 100% |
D0A9P8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
Q4QHN1 | Leishmania major | 92% | 100% |
V5BMJ5 | Trypanosoma cruzi | 37% | 100% |