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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4H3U6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 242 | 246 | PF00656 | 0.615 |
CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.669 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.516 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.429 |
CLV_PCSK_PC1ET2_1 | 267 | 269 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.514 |
DEG_SPOP_SBC_1 | 117 | 121 | PF00917 | 0.592 |
DOC_CYCLIN_RxL_1 | 194 | 204 | PF00134 | 0.398 |
DOC_MAPK_gen_1 | 201 | 209 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 53 | 59 | PF00069 | 0.420 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.568 |
DOC_USP7_UBL2_3 | 103 | 107 | PF12436 | 0.526 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.587 |
LIG_14-3-3_CanoR_1 | 201 | 209 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 46 | 51 | PF00244 | 0.521 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.730 |
LIG_BIR_III_4 | 85 | 89 | PF00653 | 0.578 |
LIG_BRCT_BRCA1_1 | 186 | 190 | PF00533 | 0.627 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.416 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.322 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.523 |
LIG_LIR_Gen_1 | 204 | 214 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 204 | 209 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.504 |
LIG_PCNA_PIPBox_1 | 134 | 143 | PF02747 | 0.548 |
LIG_PCNA_yPIPBox_3 | 89 | 103 | PF02747 | 0.669 |
LIG_SH2_CRK | 52 | 56 | PF00017 | 0.495 |
LIG_SH2_GRB2like | 78 | 81 | PF00017 | 0.603 |
LIG_SH2_PTP2 | 206 | 209 | PF00017 | 0.536 |
LIG_SH2_SRC | 158 | 161 | PF00017 | 0.517 |
LIG_SH2_SRC | 78 | 81 | PF00017 | 0.724 |
LIG_SH2_STAP1 | 141 | 145 | PF00017 | 0.524 |
LIG_SH2_STAT3 | 24 | 27 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.407 |
MOD_CDK_SPxxK_3 | 190 | 197 | PF00069 | 0.525 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.650 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.693 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.680 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.775 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.762 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.716 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.656 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.638 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.616 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.583 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.642 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.576 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.709 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.673 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.622 |
MOD_N-GLC_1 | 113 | 118 | PF02516 | 0.525 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.527 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.439 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.334 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.546 |
MOD_PKA_1 | 201 | 207 | PF00069 | 0.317 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.621 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.364 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.638 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.481 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.584 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.491 |
TRG_ER_diArg_1 | 200 | 202 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 270 | 272 | PF00400 | 0.485 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZG7 | Leptomonas seymouri | 53% | 89% |
A0A1X0NLP6 | Trypanosomatidae | 32% | 100% |
A0A3R7L3M0 | Trypanosoma rangeli | 31% | 100% |
A0A3S5H590 | Leishmania donovani | 77% | 100% |
A4HS21 | Leishmania infantum | 77% | 100% |
C9ZY14 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AK08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q9XZY6 | Leishmania major | 73% | 98% |