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 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: A4HP62
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 | 232 | 236 | PF00656 | 0.287 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.293 |
CLV_PCSK_PC1ET2_1 | 189 | 191 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.532 |
DOC_ANK_TNKS_1 | 227 | 234 | PF00023 | 0.433 |
DOC_MAPK_HePTP_8 | 151 | 163 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 154 | 163 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 349 | 357 | PF00069 | 0.630 |
DOC_MAPK_MEF2A_6 | 78 | 86 | PF00069 | 0.453 |
DOC_PP2B_LxvP_1 | 84 | 87 | PF13499 | 0.587 |
DOC_PP2B_PxIxI_1 | 155 | 161 | PF00149 | 0.449 |
DOC_PP4_FxxP_1 | 299 | 302 | PF00568 | 0.344 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.445 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.533 |
LIG_14-3-3_CanoR_1 | 150 | 158 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 206 | 211 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 295 | 300 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 303 | 312 | PF00244 | 0.363 |
LIG_Actin_WH2_2 | 317 | 332 | PF00022 | 0.503 |
LIG_APCC_ABBA_1 | 43 | 48 | PF00400 | 0.468 |
LIG_BIR_III_2 | 114 | 118 | PF00653 | 0.546 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.459 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.363 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.407 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.456 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.409 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.536 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.371 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.469 |
LIG_FHA_2 | 329 | 335 | PF00498 | 0.547 |
LIG_GBD_Chelix_1 | 108 | 116 | PF00786 | 0.526 |
LIG_LIR_Apic_2 | 297 | 302 | PF02991 | 0.346 |
LIG_LIR_Apic_2 | 30 | 36 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 124 | 133 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 143 | 151 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 175 | 185 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 20 | 29 | PF02991 | 0.693 |
LIG_LIR_Gen_1 | 252 | 262 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 124 | 128 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 143 | 147 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.413 |
LIG_PDZ_Class_1 | 366 | 371 | PF00595 | 0.713 |
LIG_Pex14_1 | 131 | 135 | PF04695 | 0.328 |
LIG_Pex14_2 | 23 | 27 | PF04695 | 0.451 |
LIG_Pex14_2 | 254 | 258 | PF04695 | 0.344 |
LIG_Pex14_2 | 281 | 285 | PF04695 | 0.344 |
LIG_Pex14_2 | 56 | 60 | PF04695 | 0.515 |
LIG_SH2_CRK | 33 | 37 | PF00017 | 0.488 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.707 |
LIG_SH2_GRB2like | 138 | 141 | PF00017 | 0.227 |
LIG_SH2_NCK_1 | 33 | 37 | PF00017 | 0.438 |
LIG_SH2_SRC | 138 | 141 | PF00017 | 0.330 |
LIG_SH2_STAP1 | 135 | 139 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.227 |
LIG_SUMO_SIM_anti_2 | 157 | 162 | PF11976 | 0.344 |
LIG_SUMO_SIM_par_1 | 82 | 88 | PF11976 | 0.531 |
LIG_TRAF2_1 | 262 | 265 | PF00917 | 0.449 |
LIG_UBA3_1 | 101 | 107 | PF00899 | 0.461 |
LIG_UBA3_1 | 158 | 164 | PF00899 | 0.449 |
MOD_CDK_SPK_2 | 163 | 168 | PF00069 | 0.474 |
MOD_CDK_SPK_2 | 298 | 303 | PF00069 | 0.227 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.366 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.291 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.466 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.538 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.773 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.536 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.363 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.433 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.369 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.329 |
MOD_DYRK1A_RPxSP_1 | 31 | 35 | PF00069 | 0.449 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.683 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.450 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.449 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.437 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.357 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.459 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.295 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.324 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.227 |
MOD_N-GLC_1 | 287 | 292 | PF02516 | 0.449 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.655 |
MOD_N-GLC_2 | 333 | 335 | PF02516 | 0.365 |
MOD_N-GLC_2 | 66 | 68 | PF02516 | 0.760 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.513 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.324 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.705 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.351 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.426 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.629 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.564 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.686 |
MOD_NEK2_2 | 22 | 27 | PF00069 | 0.447 |
MOD_OFUCOSY | 335 | 341 | PF10250 | 0.453 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.450 |
MOD_PIKK_1 | 179 | 185 | PF00454 | 0.466 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.658 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.423 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.393 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.280 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.449 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.145 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.453 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.457 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.449 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.413 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.464 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.525 |
MOD_SUMO_for_1 | 320 | 323 | PF00179 | 0.303 |
MOD_SUMO_rev_2 | 259 | 267 | PF00179 | 0.410 |
MOD_SUMO_rev_2 | 343 | 350 | PF00179 | 0.560 |
MOD_SUMO_rev_2 | 70 | 79 | PF00179 | 0.721 |
TRG_DiLeu_BaEn_1 | 98 | 103 | PF01217 | 0.446 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZW5 | Leptomonas seymouri | 60% | 100% |
A0A0S4JCM6 | Bodo saltans | 28% | 100% |
A0A0S4JIE3 | Bodo saltans | 40% | 100% |
A0A1X0P7Q9 | Trypanosomatidae | 50% | 100% |
A0A3R7M9V1 | Trypanosoma rangeli | 46% | 100% |
A0A3S7XAT0 | Leishmania donovani | 79% | 99% |
E9AG16 | Leishmania major | 78% | 100% |
E9AHX4 | Leishmania infantum | 79% | 100% |
E9ASX0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
V5BGD9 | Trypanosoma cruzi | 46% | 100% |