Distantly related to a domain found in MEAK7, a regulatory subunit of animal mTOR complex. The hydrophobic segment is likely a perimembrane anchor, not a TM region (used instead of a mirystoylation site found in mammals)
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: 1, no: 9 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9AHX4
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0004386 | helicase activity | 2 | 3 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 3 |
GO:0140657 | ATP-dependent activity | 1 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 335 | 339 | PF00656 | 0.457 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.503 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.320 |
CLV_PCSK_PC1ET2_1 | 90 | 92 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.477 |
DOC_ANK_TNKS_1 | 218 | 225 | PF00023 | 0.297 |
DOC_CKS1_1 | 47 | 52 | PF01111 | 0.548 |
DOC_CKS1_1 | 94 | 99 | PF01111 | 0.520 |
DOC_MAPK_HePTP_8 | 142 | 154 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 145 | 154 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 340 | 348 | PF00069 | 0.545 |
DOC_PP2B_PxIxI_1 | 146 | 152 | PF00149 | 0.381 |
DOC_PP4_FxxP_1 | 290 | 293 | PF00568 | 0.249 |
DOC_PP4_FxxP_1 | 47 | 50 | PF00568 | 0.549 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.387 |
DOC_USP7_UBL2_3 | 65 | 69 | PF12436 | 0.529 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.518 |
LIG_14-3-3_CanoR_1 | 141 | 149 | PF00244 | 0.234 |
LIG_14-3-3_CanoR_1 | 197 | 202 | PF00244 | 0.259 |
LIG_14-3-3_CanoR_1 | 286 | 291 | PF00244 | 0.271 |
LIG_14-3-3_CanoR_1 | 294 | 303 | PF00244 | 0.268 |
LIG_BIR_III_2 | 105 | 109 | PF00653 | 0.388 |
LIG_BRCT_BRCA1_1 | 205 | 209 | PF00533 | 0.292 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.311 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.268 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.302 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.360 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.641 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.434 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.420 |
LIG_GBD_Chelix_1 | 99 | 107 | PF00786 | 0.371 |
LIG_LIR_Apic_2 | 22 | 27 | PF02991 | 0.362 |
LIG_LIR_Apic_2 | 288 | 293 | PF02991 | 0.252 |
LIG_LIR_Apic_2 | 46 | 50 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 134 | 142 | PF02991 | 0.228 |
LIG_LIR_Gen_1 | 166 | 173 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 243 | 253 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 3 | 12 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 134 | 138 | PF02991 | 0.170 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.247 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.544 |
LIG_MLH1_MIPbox_1 | 21 | 25 | PF16413 | 0.311 |
LIG_PDZ_Class_1 | 357 | 362 | PF00595 | 0.585 |
LIG_Pex14_1 | 122 | 126 | PF04695 | 0.290 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.249 |
LIG_Pex14_2 | 272 | 276 | PF04695 | 0.249 |
LIG_REV1ctd_RIR_1 | 269 | 279 | PF16727 | 0.147 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.565 |
LIG_SH2_PTP2 | 8 | 11 | PF00017 | 0.315 |
LIG_SH2_SRC | 12 | 15 | PF00017 | 0.288 |
LIG_SH2_SRC | 129 | 132 | PF00017 | 0.234 |
LIG_SH2_SRC | 221 | 224 | PF00017 | 0.247 |
LIG_SH2_SRC | 8 | 11 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.315 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.671 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.289 |
LIG_SUMO_SIM_anti_2 | 148 | 153 | PF11976 | 0.268 |
LIG_SUMO_SIM_par_1 | 91 | 96 | PF11976 | 0.354 |
LIG_TRAF2_1 | 253 | 256 | PF00917 | 0.381 |
LIG_TRAF2_1 | 64 | 67 | PF00917 | 0.659 |
LIG_UBA3_1 | 149 | 155 | PF00899 | 0.381 |
LIG_UBA3_1 | 92 | 98 | PF00899 | 0.341 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.313 |
MOD_CDK_SPK_2 | 154 | 159 | PF00069 | 0.322 |
MOD_CDK_SPK_2 | 93 | 98 | PF00069 | 0.350 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.467 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.322 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.405 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.602 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.731 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.184 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.372 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.292 |
MOD_Cter_Amidation | 88 | 91 | PF01082 | 0.243 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.418 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.252 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.236 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.328 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.640 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.395 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.379 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.266 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.338 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.406 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.312 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.322 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.489 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.666 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.555 |
MOD_N-GLC_2 | 57 | 59 | PF02516 | 0.596 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.252 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.365 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.487 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.608 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.306 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.234 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.344 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.312 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.287 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.244 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.553 |
MOD_Plk_2-3 | 227 | 233 | PF00069 | 0.247 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.361 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.214 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.357 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.346 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.418 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.395 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.407 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.717 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.474 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.512 |
MOD_SUMO_for_1 | 64 | 67 | PF00179 | 0.580 |
MOD_SUMO_rev_2 | 250 | 258 | PF00179 | 0.328 |
MOD_SUMO_rev_2 | 61 | 70 | PF00179 | 0.656 |
TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.310 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZW5 | Leptomonas seymouri | 61% | 100% |
A0A0S4JCM6 | Bodo saltans | 25% | 100% |
A0A0S4JIE3 | Bodo saltans | 42% | 100% |
A0A1X0P7Q9 | Trypanosomatidae | 49% | 100% |
A0A3R7M9V1 | Trypanosoma rangeli | 46% | 100% |
A0A3S7XAT0 | Leishmania donovani | 96% | 97% |
A4HP62 | Leishmania braziliensis | 79% | 100% |
E9AG16 | Leishmania major | 89% | 100% |
E9ASX0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q8K0P3 | Mus musculus | 28% | 80% |
V5BGD9 | Trypanosoma cruzi | 46% | 99% |