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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0035869 | ciliary transition zone | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H7H3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.762 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.688 |
CLV_PCSK_FUR_1 | 290 | 294 | PF00082 | 0.750 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.610 |
CLV_PCSK_PC1ET2_1 | 292 | 294 | PF00082 | 0.721 |
DEG_ODPH_VHL_1 | 56 | 69 | PF01847 | 0.518 |
DEG_SCF_FBW7_1 | 69 | 75 | PF00400 | 0.512 |
DOC_CDC14_PxL_1 | 56 | 64 | PF14671 | 0.515 |
DOC_CKS1_1 | 69 | 74 | PF01111 | 0.508 |
DOC_CYCLIN_yCln2_LP_2 | 5 | 11 | PF00134 | 0.539 |
DOC_CYCLIN_yCln2_LP_2 | 50 | 56 | PF00134 | 0.651 |
DOC_PP2B_LxvP_1 | 31 | 34 | PF13499 | 0.563 |
DOC_PP2B_LxvP_1 | 48 | 51 | PF13499 | 0.720 |
DOC_PP2B_LxvP_1 | 5 | 8 | PF13499 | 0.526 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.630 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.598 |
LIG_14-3-3_CanoR_1 | 182 | 191 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 201 | 206 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 259 | 267 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 282 | 287 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 315 | 321 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 323 | 332 | PF00244 | 0.682 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.578 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.522 |
LIG_EH1_1 | 156 | 164 | PF00400 | 0.470 |
LIG_eIF4E_1 | 157 | 163 | PF01652 | 0.511 |
LIG_eIF4E_1 | 307 | 313 | PF01652 | 0.747 |
LIG_EVH1_1 | 31 | 35 | PF00568 | 0.560 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.598 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.539 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.696 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.774 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.417 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.646 |
LIG_LIR_Gen_1 | 135 | 144 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 227 | 237 | PF02991 | 0.650 |
LIG_LIR_Gen_1 | 261 | 271 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 135 | 140 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 261 | 266 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.630 |
LIG_MYND_1 | 43 | 47 | PF01753 | 0.510 |
LIG_RPA_C_Fungi | 204 | 216 | PF08784 | 0.608 |
LIG_SH2_CRK | 332 | 336 | PF00017 | 0.688 |
LIG_SH2_STAP1 | 263 | 267 | PF00017 | 0.519 |
LIG_SH2_STAT3 | 197 | 200 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.615 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.594 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.589 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.668 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.699 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.557 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.691 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.633 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.662 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.705 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.788 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.590 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.733 |
LIG_SUMO_SIM_par_1 | 111 | 116 | PF11976 | 0.681 |
LIG_SUMO_SIM_par_1 | 245 | 251 | PF11976 | 0.491 |
LIG_TRAF2_1 | 139 | 142 | PF00917 | 0.622 |
LIG_TRAF2_1 | 204 | 207 | PF00917 | 0.424 |
LIG_TRFH_1 | 332 | 336 | PF08558 | 0.489 |
LIG_TYR_ITSM | 133 | 140 | PF00017 | 0.597 |
MOD_CDK_SPxxK_3 | 275 | 282 | PF00069 | 0.672 |
MOD_CDK_SPxxK_3 | 283 | 290 | PF00069 | 0.781 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.416 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.651 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.602 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.513 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.725 |
MOD_Cter_Amidation | 288 | 291 | PF01082 | 0.674 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.731 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.569 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.789 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.561 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.488 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.655 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.513 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.450 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.415 |
MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.652 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.641 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.575 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.575 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.599 |
MOD_PIKK_1 | 189 | 195 | PF00454 | 0.577 |
MOD_PK_1 | 201 | 207 | PF00069 | 0.447 |
MOD_PKA_1 | 282 | 288 | PF00069 | 0.524 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.549 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.563 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.557 |
MOD_PKB_1 | 199 | 207 | PF00069 | 0.455 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.448 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.447 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.412 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.671 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.619 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.542 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.630 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.666 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.792 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.602 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 263 | 266 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.692 |
TRG_ER_diArg_1 | 282 | 284 | PF00400 | 0.769 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.772 |
TRG_ER_diArg_1 | 313 | 315 | PF00400 | 0.731 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.638 |
TRG_NLS_Bipartite_1 | 274 | 295 | PF00514 | 0.509 |
TRG_NLS_MonoExtN_4 | 290 | 295 | PF00514 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 136 | 141 | PF00026 | 0.582 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCY4 | Leptomonas seymouri | 65% | 92% |
A0A1X0NPB8 | Trypanosomatidae | 36% | 70% |
A0A3Q8I9R2 | Leishmania donovani | 75% | 95% |
A4HVV4 | Leishmania infantum | 74% | 95% |
C9ZT73 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 67% |
E9APK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 96% |
Q4QFX3 | Leishmania major | 76% | 100% |