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: 10 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H3B2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.569 |
CLV_C14_Caspase3-7 | 186 | 190 | PF00656 | 0.686 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.636 |
CLV_PCSK_FUR_1 | 349 | 353 | PF00082 | 0.530 |
CLV_PCSK_FUR_1 | 74 | 78 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.542 |
CLV_PCSK_PC1ET2_1 | 348 | 350 | PF00082 | 0.630 |
CLV_PCSK_PC1ET2_1 | 61 | 63 | PF00082 | 0.655 |
CLV_PCSK_PC7_1 | 69 | 75 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.626 |
DOC_CKS1_1 | 283 | 288 | PF01111 | 0.488 |
DOC_MAPK_gen_1 | 73 | 83 | PF00069 | 0.572 |
DOC_MAPK_MEF2A_6 | 76 | 85 | PF00069 | 0.537 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.785 |
DOC_USP7_UBL2_3 | 29 | 33 | PF12436 | 0.602 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.499 |
LIG_14-3-3_CanoR_1 | 222 | 229 | PF00244 | 0.509 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.615 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.576 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.505 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.465 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.500 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.552 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.487 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.550 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.484 |
LIG_Integrin_isoDGR_2 | 108 | 110 | PF01839 | 0.377 |
LIG_Integrin_isoDGR_2 | 37 | 39 | PF01839 | 0.624 |
LIG_LIR_Gen_1 | 207 | 217 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 22 | 30 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 80 | 89 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 207 | 212 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 294 | 299 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 80 | 85 | PF02991 | 0.520 |
LIG_NRP_CendR_1 | 350 | 353 | PF00754 | 0.756 |
LIG_Pex14_2 | 292 | 296 | PF04695 | 0.487 |
LIG_SH2_NCK_1 | 160 | 164 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.471 |
LIG_TRAF2_1 | 11 | 14 | PF00917 | 0.550 |
LIG_TRAF2_1 | 148 | 151 | PF00917 | 0.497 |
LIG_UBA3_1 | 24 | 33 | PF00899 | 0.541 |
MOD_CDK_SPK_2 | 282 | 287 | PF00069 | 0.499 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.545 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.788 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.645 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.655 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.511 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.475 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.410 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.484 |
MOD_Cter_Amidation | 346 | 349 | PF01082 | 0.731 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.452 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.593 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.504 |
MOD_GlcNHglycan | 303 | 307 | PF01048 | 0.588 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.449 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.714 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.565 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.557 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.594 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.503 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.557 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.472 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.649 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.606 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.715 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.544 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.556 |
MOD_N-GLC_1 | 341 | 346 | PF02516 | 0.728 |
MOD_N-GLC_2 | 182 | 184 | PF02516 | 0.417 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.558 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.540 |
MOD_PIKK_1 | 271 | 277 | PF00454 | 0.587 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.712 |
MOD_PK_1 | 77 | 83 | PF00069 | 0.640 |
MOD_PKA_1 | 61 | 67 | PF00069 | 0.644 |
MOD_PKA_1 | 68 | 74 | PF00069 | 0.596 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.486 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.463 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.488 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.481 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.610 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.589 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.552 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.652 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.508 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.560 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.567 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.492 |
TRG_DiLeu_BaEn_1 | 13 | 18 | PF01217 | 0.554 |
TRG_DiLeu_BaEn_4 | 13 | 19 | PF01217 | 0.572 |
TRG_ER_diArg_1 | 116 | 118 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 269 | 272 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 349 | 352 | PF00400 | 0.695 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.715 |
TRG_ER_diArg_1 | 73 | 76 | PF00400 | 0.696 |
TRG_NLS_MonoCore_2 | 347 | 352 | PF00514 | 0.750 |
TRG_NLS_MonoExtC_3 | 347 | 352 | PF00514 | 0.671 |
TRG_Pf-PMV_PEXEL_1 | 110 | 115 | PF00026 | 0.472 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWM5 | Leptomonas seymouri | 61% | 100% |
A0A0S4JHT8 | Bodo saltans | 27% | 99% |
A0A1X0NKG5 | Trypanosomatidae | 38% | 90% |
A0A3S5H4Y1 | Leishmania donovani | 77% | 100% |
A0A422N6Z1 | Trypanosoma rangeli | 39% | 91% |
A4HRL2 | Leishmania infantum | 77% | 100% |
C9ZJ00 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 91% |
E9AC84 | Leishmania major | 77% | 100% |
E9AJH6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
V5B685 | Trypanosoma cruzi | 40% | 90% |