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: A4H4U7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.758 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.702 |
CLV_PCSK_FUR_1 | 297 | 301 | PF00082 | 0.795 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.693 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.346 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.728 |
CLV_PCSK_PC1ET2_1 | 296 | 298 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.690 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.813 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.422 |
DEG_APCC_DBOX_1 | 211 | 219 | PF00400 | 0.688 |
DOC_CKS1_1 | 266 | 271 | PF01111 | 0.571 |
DOC_MAPK_DCC_7 | 106 | 116 | PF00069 | 0.353 |
DOC_MAPK_gen_1 | 102 | 112 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 296 | 306 | PF00069 | 0.697 |
DOC_MAPK_gen_1 | 54 | 62 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 105 | 114 | PF00069 | 0.487 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.503 |
DOC_USP7_UBL2_3 | 139 | 143 | PF12436 | 0.513 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.619 |
LIG_14-3-3_CanoR_1 | 100 | 107 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 118 | 122 | PF00244 | 0.294 |
LIG_14-3-3_CanoR_1 | 169 | 177 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 225 | 235 | PF00244 | 0.672 |
LIG_Actin_WH2_2 | 103 | 120 | PF00022 | 0.584 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.588 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.476 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.467 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.586 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.671 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.802 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.357 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.603 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.332 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.734 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.723 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.605 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.429 |
LIG_LIR_Gen_1 | 74 | 84 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.443 |
LIG_NRBOX | 85 | 91 | PF00104 | 0.535 |
LIG_SH2_NCK_1 | 185 | 189 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.597 |
LIG_SH3_1 | 263 | 269 | PF00018 | 0.573 |
LIG_SH3_2 | 307 | 312 | PF14604 | 0.702 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.436 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.802 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.707 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.684 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.713 |
LIG_SUMO_SIM_par_1 | 287 | 293 | PF11976 | 0.677 |
LIG_SUMO_SIM_par_1 | 81 | 88 | PF11976 | 0.319 |
LIG_SxIP_EBH_1 | 225 | 238 | PF03271 | 0.744 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.663 |
LIG_UBA3_1 | 288 | 296 | PF00899 | 0.670 |
MOD_CDC14_SPxK_1 | 293 | 296 | PF00782 | 0.670 |
MOD_CDC14_SPxK_1 | 309 | 312 | PF00782 | 0.707 |
MOD_CDK_SPxK_1 | 290 | 296 | PF00069 | 0.671 |
MOD_CDK_SPxK_1 | 306 | 312 | PF00069 | 0.702 |
MOD_CDK_SPxxK_3 | 205 | 212 | PF00069 | 0.534 |
MOD_CDK_SPxxK_3 | 290 | 297 | PF00069 | 0.672 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.604 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.810 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.600 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.713 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.594 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.608 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.427 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.665 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.622 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.532 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.658 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.624 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.678 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.456 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.584 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.654 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.684 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.662 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.439 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.600 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.553 |
MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.509 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.521 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.479 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.605 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.597 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.449 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.580 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.748 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.497 |
MOD_PKB_1 | 298 | 306 | PF00069 | 0.763 |
MOD_PKB_1 | 98 | 106 | PF00069 | 0.606 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.526 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.803 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.565 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.627 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.676 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.453 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.468 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.695 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.649 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.761 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.671 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.702 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.615 |
MOD_SUMO_rev_2 | 193 | 200 | PF00179 | 0.769 |
TRG_DiLeu_BaEn_1 | 57 | 62 | PF01217 | 0.606 |
TRG_ER_diArg_1 | 240 | 242 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.692 |
TRG_NLS_Bipartite_1 | 225 | 243 | PF00514 | 0.748 |
TRG_NLS_MonoCore_2 | 238 | 243 | PF00514 | 0.754 |
TRG_NLS_MonoCore_2 | 295 | 300 | PF00514 | 0.676 |
TRG_NLS_MonoExtC_3 | 238 | 244 | PF00514 | 0.755 |
TRG_NLS_MonoExtC_3 | 295 | 300 | PF00514 | 0.686 |
TRG_NLS_MonoExtN_4 | 294 | 300 | PF00514 | 0.684 |
TRG_Pf-PMV_PEXEL_1 | 59 | 64 | PF00026 | 0.459 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZD5 | Leptomonas seymouri | 41% | 100% |
A0A3S7WPQ1 | Leishmania donovani | 73% | 100% |
A4HT26 | Leishmania infantum | 73% | 100% |
E9AL14 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 99% |
Q4QIU0 | Leishmania major | 74% | 100% |