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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4H8L3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.504 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.750 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.620 |
CLV_Separin_Metazoa | 233 | 237 | PF03568 | 0.436 |
DEG_SPOP_SBC_1 | 268 | 272 | PF00917 | 0.642 |
DOC_CKS1_1 | 254 | 259 | PF01111 | 0.490 |
DOC_CKS1_1 | 287 | 292 | PF01111 | 0.528 |
DOC_MAPK_gen_1 | 30 | 38 | PF00069 | 0.551 |
DOC_PP1_RVXF_1 | 97 | 104 | PF00149 | 0.528 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.565 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 171 | 177 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 18 | 22 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 275 | 285 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 46 | 54 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 99 | 104 | PF00244 | 0.538 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.569 |
LIG_BRCT_BRCA1_1 | 205 | 209 | PF00533 | 0.527 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.556 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.440 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.493 |
LIG_LIR_Gen_1 | 105 | 111 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 138 | 146 | PF02991 | 0.602 |
LIG_LIR_Gen_1 | 20 | 28 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 20 | 24 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.515 |
LIG_LYPXL_yS_3 | 53 | 56 | PF13949 | 0.475 |
LIG_PDZ_Class_2 | 293 | 298 | PF00595 | 0.478 |
LIG_Pex14_1 | 103 | 107 | PF04695 | 0.493 |
LIG_Rb_LxCxE_1 | 117 | 138 | PF01857 | 0.576 |
LIG_SH2_CRK | 167 | 171 | PF00017 | 0.598 |
LIG_SH2_CRK | 288 | 292 | PF00017 | 0.493 |
LIG_SH2_NCK_1 | 70 | 74 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.477 |
LIG_SH3_1 | 167 | 173 | PF00018 | 0.596 |
LIG_SH3_1 | 281 | 287 | PF00018 | 0.517 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.556 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.465 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.592 |
LIG_TYR_ITSM | 49 | 56 | PF00017 | 0.474 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.520 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.613 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.547 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.616 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.683 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.667 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.500 |
MOD_Cter_Amidation | 16 | 19 | PF01082 | 0.479 |
MOD_Cter_Amidation | 190 | 193 | PF01082 | 0.570 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.607 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.662 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.556 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.478 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.599 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.655 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.532 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.709 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.504 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.542 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.531 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.609 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.703 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.600 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.523 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.590 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.624 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.615 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.609 |
MOD_PKA_1 | 99 | 105 | PF00069 | 0.508 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.492 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.525 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.488 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.485 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.647 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.410 |
MOD_PKB_1 | 192 | 200 | PF00069 | 0.569 |
MOD_PKB_1 | 66 | 74 | PF00069 | 0.495 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.672 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.530 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.548 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.662 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.633 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.547 |
TRG_ER_diArg_1 | 119 | 122 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 169 | 172 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 65 | 68 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P756 | Leptomonas seymouri | 33% | 96% |
A0A3S7WU02 | Leishmania donovani | 70% | 100% |
E9AGN6 | Leishmania infantum | 71% | 100% |
E9AQP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 100% |
Q4QES9 | Leishmania major | 68% | 100% |