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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HN53
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.353 |
CLV_PCSK_FUR_1 | 15 | 19 | PF00082 | 0.487 |
CLV_PCSK_FUR_1 | 264 | 268 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 266 | 268 | PF00082 | 0.513 |
CLV_PCSK_PC7_1 | 13 | 19 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.469 |
DEG_APCC_DBOX_1 | 160 | 168 | PF00400 | 0.500 |
DEG_APCC_DBOX_1 | 316 | 324 | PF00400 | 0.462 |
DEG_SCF_FBW7_1 | 167 | 172 | PF00400 | 0.499 |
DEG_SPOP_SBC_1 | 331 | 335 | PF00917 | 0.480 |
DOC_CDC14_PxL_1 | 24 | 32 | PF14671 | 0.472 |
DOC_CKS1_1 | 340 | 345 | PF01111 | 0.496 |
DOC_CYCLIN_RxL_1 | 103 | 116 | PF00134 | 0.428 |
DOC_MAPK_gen_1 | 103 | 112 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 264 | 271 | PF00069 | 0.494 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.453 |
DOC_USP7_UBL2_3 | 301 | 305 | PF12436 | 0.472 |
DOC_USP7_UBL2_3 | 87 | 91 | PF12436 | 0.327 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.490 |
LIG_14-3-3_CanoR_1 | 196 | 206 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 228 | 236 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 259 | 265 | PF00244 | 0.448 |
LIG_Actin_WH2_2 | 287 | 303 | PF00022 | 0.497 |
LIG_Actin_WH2_2 | 97 | 115 | PF00022 | 0.449 |
LIG_Clathr_ClatBox_1 | 323 | 327 | PF01394 | 0.480 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.591 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.499 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.477 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.514 |
LIG_LIR_Apic_2 | 345 | 349 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 149 | 160 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 123 | 128 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 149 | 155 | PF02991 | 0.699 |
LIG_NRBOX | 319 | 325 | PF00104 | 0.473 |
LIG_SH2_CRK | 125 | 129 | PF00017 | 0.339 |
LIG_SH2_CRK | 31 | 35 | PF00017 | 0.450 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.495 |
LIG_SUMO_SIM_anti_2 | 203 | 210 | PF11976 | 0.497 |
LIG_TRAF2_1 | 201 | 204 | PF00917 | 0.459 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.706 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.484 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.558 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.501 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.510 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.360 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.575 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.743 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.698 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.492 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.315 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.352 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.477 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.658 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.695 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.494 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.380 |
MOD_N-GLC_1 | 228 | 233 | PF02516 | 0.575 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.524 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.485 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.485 |
MOD_NEK2_2 | 133 | 138 | PF00069 | 0.460 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.480 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.506 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.559 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.642 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.684 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.544 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.478 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.481 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.560 |
MOD_Plk_2-3 | 141 | 147 | PF00069 | 0.420 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.501 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.473 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.703 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.493 |
MOD_SUMO_for_1 | 90 | 93 | PF00179 | 0.316 |
TRG_DiLeu_BaEn_1 | 204 | 209 | PF01217 | 0.500 |
TRG_DiLeu_BaEn_4 | 92 | 98 | PF01217 | 0.390 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.458 |
TRG_ER_diArg_1 | 15 | 18 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.482 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3I4 | Leptomonas seymouri | 37% | 100% |
A0A3Q8IIM5 | Leishmania donovani | 75% | 100% |
A0A3R7NA43 | Trypanosoma rangeli | 29% | 96% |
A4IBS0 | Leishmania infantum | 75% | 100% |
E9AFK6 | Leishmania major | 74% | 100% |
E9B6R0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |