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: 10 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A0A3S7XAT0
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 | 10 | 14 | PF00656 | 0.346 |
CLV_C14_Caspase3-7 | 347 | 351 | PF00656 | 0.658 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.516 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.516 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.346 |
DOC_ANK_TNKS_1 | 230 | 237 | PF00023 | 0.378 |
DOC_CKS1_1 | 106 | 111 | PF01111 | 0.550 |
DOC_CKS1_1 | 59 | 64 | PF01111 | 0.641 |
DOC_MAPK_HePTP_8 | 154 | 166 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 157 | 166 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 352 | 360 | PF00069 | 0.611 |
DOC_PP2B_PxIxI_1 | 158 | 164 | PF00149 | 0.432 |
DOC_PP4_FxxP_1 | 302 | 305 | PF00568 | 0.312 |
DOC_PP4_FxxP_1 | 59 | 62 | PF00568 | 0.647 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.431 |
DOC_USP7_UBL2_3 | 77 | 81 | PF12436 | 0.616 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.339 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.540 |
LIG_14-3-3_CanoR_1 | 153 | 161 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 209 | 214 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 298 | 303 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 306 | 315 | PF00244 | 0.332 |
LIG_BIR_III_2 | 117 | 121 | PF00653 | 0.480 |
LIG_BRCT_BRCA1_1 | 217 | 221 | PF00533 | 0.318 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.471 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.332 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.345 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.416 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.344 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.689 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.410 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.459 |
LIG_GBD_Chelix_1 | 111 | 119 | PF00786 | 0.461 |
LIG_LIR_Apic_2 | 300 | 305 | PF02991 | 0.319 |
LIG_LIR_Apic_2 | 58 | 62 | PF02991 | 0.644 |
LIG_LIR_Gen_1 | 146 | 154 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 17 | 27 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 178 | 185 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 255 | 265 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 30 | 39 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 13 | 19 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 146 | 150 | PF02991 | 0.236 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 220 | 225 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 255 | 260 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 30 | 34 | PF02991 | 0.516 |
LIG_PDZ_Class_1 | 369 | 374 | PF00595 | 0.688 |
LIG_Pex14_1 | 134 | 138 | PF04695 | 0.315 |
LIG_Pex14_2 | 257 | 261 | PF04695 | 0.312 |
LIG_Pex14_2 | 284 | 288 | PF04695 | 0.328 |
LIG_SH2_CRK | 31 | 35 | PF00017 | 0.383 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.656 |
LIG_SH2_PTP2 | 19 | 22 | PF00017 | 0.351 |
LIG_SH2_PTP2 | 35 | 38 | PF00017 | 0.356 |
LIG_SH2_SRC | 141 | 144 | PF00017 | 0.295 |
LIG_SH2_SRC | 19 | 22 | PF00017 | 0.351 |
LIG_SH2_SRC | 233 | 236 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 138 | 142 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 29 | 33 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.391 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.230 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.553 |
LIG_SUMO_SIM_anti_2 | 160 | 165 | PF11976 | 0.312 |
LIG_SUMO_SIM_par_1 | 103 | 108 | PF11976 | 0.526 |
LIG_TRAF2_1 | 265 | 268 | PF00917 | 0.432 |
LIG_TRAF2_1 | 76 | 79 | PF00917 | 0.707 |
LIG_TYR_ITIM | 33 | 38 | PF00017 | 0.386 |
LIG_UBA3_1 | 104 | 110 | PF00899 | 0.412 |
LIG_UBA3_1 | 161 | 167 | PF00899 | 0.432 |
MOD_CDK_SPK_2 | 105 | 110 | PF00069 | 0.506 |
MOD_CDK_SPK_2 | 166 | 171 | PF00069 | 0.411 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.524 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.352 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.435 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.644 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.410 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.786 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.413 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.235 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.378 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.337 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.506 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.317 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.293 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.312 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.693 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.410 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.432 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.417 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.145 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.316 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.390 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.357 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.360 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.538 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.681 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.614 |
MOD_N-GLC_2 | 69 | 71 | PF02516 | 0.707 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.462 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.298 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.406 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.521 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.681 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.295 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.383 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.302 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.348 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.298 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.613 |
MOD_Plk_2-3 | 239 | 245 | PF00069 | 0.312 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.402 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.303 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.145 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.424 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.438 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.469 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.334 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.432 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.780 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.531 |
MOD_SUMO_for_1 | 76 | 79 | PF00179 | 0.656 |
MOD_SUMO_rev_2 | 262 | 270 | PF00179 | 0.388 |
MOD_SUMO_rev_2 | 73 | 82 | PF00179 | 0.718 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 35 | 38 | PF00928 | 0.379 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZW5 | Leptomonas seymouri | 61% | 100% |
A0A0S4JCM6 | Bodo saltans | 26% | 100% |
A0A0S4JIE3 | Bodo saltans | 42% | 100% |
A0A1X0P7Q9 | Trypanosomatidae | 49% | 100% |
A0A3R7M9V1 | Trypanosoma rangeli | 46% | 100% |
A4HP62 | Leishmania braziliensis | 79% | 100% |
E9AG16 | Leishmania major | 85% | 100% |
E9AHX4 | Leishmania infantum | 96% | 100% |
E9ASX0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BGD9 | Trypanosoma cruzi | 47% | 100% |