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: 2 |
NetGPI | no | yes: 0, no: 2 |
Related structures:
AlphaFold database: A4H3H0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 140 | 144 | PF00656 | 0.743 |
CLV_C14_Caspase3-7 | 234 | 238 | PF00656 | 0.732 |
CLV_C14_Caspase3-7 | 332 | 336 | PF00656 | 0.635 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.722 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.742 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.742 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.738 |
CLV_PCSK_PC1ET2_1 | 136 | 138 | PF00082 | 0.742 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.742 |
CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.639 |
CLV_PCSK_PC1ET2_1 | 46 | 48 | PF00082 | 0.738 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.709 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.820 |
DOC_MAPK_gen_1 | 189 | 199 | PF00069 | 0.711 |
DOC_MAPK_gen_1 | 285 | 297 | PF00069 | 0.710 |
DOC_MAPK_gen_1 | 383 | 395 | PF00069 | 0.598 |
DOC_MAPK_gen_1 | 91 | 101 | PF00069 | 0.706 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.702 |
DOC_USP7_UBL2_3 | 286 | 290 | PF12436 | 0.705 |
DOC_USP7_UBL2_3 | 384 | 388 | PF12436 | 0.590 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.716 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.604 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.679 |
LIG_LIR_Apic_2 | 128 | 134 | PF02991 | 0.693 |
LIG_PTB_Apo_2 | 170 | 177 | PF02174 | 0.695 |
LIG_PTB_Apo_2 | 268 | 275 | PF02174 | 0.697 |
LIG_PTB_Apo_2 | 72 | 79 | PF02174 | 0.683 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.695 |
LIG_SH2_SRC | 167 | 170 | PF00017 | 0.695 |
LIG_SH2_SRC | 222 | 225 | PF00017 | 0.701 |
LIG_SH2_SRC | 26 | 29 | PF00017 | 0.698 |
LIG_SH2_SRC | 265 | 268 | PF00017 | 0.700 |
LIG_SH2_SRC | 363 | 366 | PF00017 | 0.596 |
LIG_SH2_SRC | 69 | 72 | PF00017 | 0.689 |
LIG_SH2_STAP1 | 167 | 171 | PF00017 | 0.694 |
LIG_SH2_STAP1 | 265 | 269 | PF00017 | 0.698 |
LIG_SH2_STAP1 | 363 | 367 | PF00017 | 0.593 |
LIG_SH2_STAP1 | 69 | 73 | PF00017 | 0.685 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.718 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.719 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.701 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.698 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.718 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.722 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.711 |
LIG_SUMO_SIM_par_1 | 107 | 113 | PF11976 | 0.606 |
LIG_SUMO_SIM_par_1 | 9 | 15 | PF11976 | 0.681 |
LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.710 |
LIG_TRAF2_1 | 225 | 228 | PF00917 | 0.706 |
LIG_TRAF2_1 | 29 | 32 | PF00917 | 0.699 |
LIG_TRAF2_1 | 323 | 326 | PF00917 | 0.724 |
MOD_CDC14_SPxK_1 | 133 | 136 | PF00782 | 0.714 |
MOD_CDK_SPK_2 | 130 | 135 | PF00069 | 0.695 |
MOD_CDK_SPK_2 | 228 | 233 | PF00069 | 0.715 |
MOD_CDK_SPK_2 | 32 | 37 | PF00069 | 0.709 |
MOD_CDK_SPK_2 | 326 | 331 | PF00069 | 0.716 |
MOD_CDK_SPxK_1 | 130 | 136 | PF00069 | 0.700 |
MOD_CDK_SPxxK_3 | 130 | 137 | PF00069 | 0.707 |
MOD_CDK_SPxxK_3 | 228 | 235 | PF00069 | 0.722 |
MOD_CDK_SPxxK_3 | 32 | 39 | PF00069 | 0.716 |
MOD_CDK_SPxxK_3 | 326 | 333 | PF00069 | 0.722 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.714 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.705 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.699 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.722 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.696 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.706 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.705 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.735 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.705 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.737 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.810 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.735 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.731 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.680 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.746 |
MOD_PIKK_1 | 235 | 241 | PF00454 | 0.731 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.736 |
MOD_PIKK_1 | 39 | 45 | PF00454 | 0.731 |
MOD_PK_1 | 212 | 218 | PF00069 | 0.694 |
MOD_PKB_1 | 135 | 143 | PF00069 | 0.745 |
MOD_PKB_1 | 233 | 241 | PF00069 | 0.732 |
MOD_PKB_1 | 331 | 339 | PF00069 | 0.736 |
MOD_PKB_1 | 37 | 45 | PF00069 | 0.731 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.700 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.718 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.713 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.719 |
MOD_SUMO_rev_2 | 145 | 154 | PF00179 | 0.740 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.695 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.700 |
TRG_ENDOCYTIC_2 | 363 | 366 | PF00928 | 0.596 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.689 |
TRG_ER_diArg_1 | 134 | 137 | PF00400 | 0.730 |
TRG_ER_diLys_1 | 396 | 399 | PF00400 | 0.607 |
TRG_NLS_Bipartite_1 | 120 | 140 | PF00514 | 0.715 |
TRG_NLS_MonoExtC_3 | 134 | 139 | PF00514 | 0.736 |
TRG_NLS_MonoExtN_4 | 134 | 140 | PF00514 | 0.737 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A4H3G3 | Leishmania braziliensis | 96% | 100% |