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: E9ASX0
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 | 342 | 346 | PF00656 | 0.663 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.527 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.477 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.363 |
DOC_CKS1_1 | 54 | 59 | PF01111 | 0.645 |
DOC_MAPK_HePTP_8 | 149 | 161 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 152 | 161 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 347 | 355 | PF00069 | 0.599 |
DOC_PP2B_PxIxI_1 | 153 | 159 | PF00149 | 0.420 |
DOC_PP4_FxxP_1 | 297 | 300 | PF00568 | 0.309 |
DOC_PP4_FxxP_1 | 54 | 57 | PF00568 | 0.645 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.401 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.230 |
DOC_USP7_UBL2_3 | 72 | 76 | PF12436 | 0.646 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.510 |
LIG_14-3-3_CanoR_1 | 204 | 209 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 293 | 298 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 301 | 310 | PF00244 | 0.328 |
LIG_Actin_WH2_2 | 315 | 330 | PF00022 | 0.491 |
LIG_BIR_III_2 | 112 | 116 | PF00653 | 0.521 |
LIG_BRCT_BRCA1_1 | 212 | 216 | PF00533 | 0.331 |
LIG_FAT_LD_1 | 34 | 42 | PF03623 | 0.283 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.432 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.328 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.461 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.379 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.243 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.674 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.603 |
LIG_GBD_Chelix_1 | 106 | 114 | PF00786 | 0.501 |
LIG_LIR_Apic_2 | 295 | 300 | PF02991 | 0.311 |
LIG_LIR_Apic_2 | 53 | 57 | PF02991 | 0.638 |
LIG_LIR_Gen_1 | 141 | 149 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 173 | 180 | PF02991 | 0.296 |
LIG_LIR_Gen_1 | 20 | 31 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 250 | 260 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 6 | 15 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 141 | 145 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 20 | 24 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 250 | 255 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 6 | 10 | PF02991 | 0.496 |
LIG_NRBOX | 33 | 39 | PF00104 | 0.266 |
LIG_PDZ_Class_1 | 364 | 369 | PF00595 | 0.733 |
LIG_Pex14_1 | 129 | 133 | PF04695 | 0.309 |
LIG_Pex14_2 | 252 | 256 | PF04695 | 0.309 |
LIG_Pex14_2 | 279 | 283 | PF04695 | 0.309 |
LIG_SH2_CRK | 21 | 25 | PF00017 | 0.408 |
LIG_SH2_CRK | 29 | 33 | PF00017 | 0.475 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.468 |
LIG_SH2_CRK | 78 | 82 | PF00017 | 0.697 |
LIG_SH2_PTP2 | 11 | 14 | PF00017 | 0.336 |
LIG_SH2_PTP2 | 15 | 18 | PF00017 | 0.320 |
LIG_SH2_SRC | 11 | 14 | PF00017 | 0.336 |
LIG_SH2_SRC | 15 | 18 | PF00017 | 0.320 |
LIG_SH2_STAP1 | 133 | 137 | PF00017 | 0.381 |
LIG_SH2_STAP1 | 29 | 33 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.293 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.627 |
LIG_SUMO_SIM_anti_2 | 155 | 160 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 98 | 103 | PF11976 | 0.431 |
LIG_TRAF2_1 | 260 | 263 | PF00917 | 0.420 |
LIG_TRAF2_1 | 71 | 74 | PF00917 | 0.713 |
LIG_TYR_ITIM | 27 | 32 | PF00017 | 0.255 |
LIG_TYR_ITIM | 9 | 14 | PF00017 | 0.272 |
LIG_UBA3_1 | 156 | 162 | PF00899 | 0.401 |
LIG_UBA3_1 | 99 | 105 | PF00899 | 0.415 |
LIG_WRC_WIRS_1 | 133 | 138 | PF05994 | 0.372 |
MOD_CDK_SPK_2 | 100 | 105 | PF00069 | 0.533 |
MOD_CDK_SPK_2 | 161 | 166 | PF00069 | 0.452 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.472 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.344 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.333 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.429 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.641 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.737 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.352 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.722 |
MOD_GlcNHglycan | 122 | 126 | PF01048 | 0.536 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.396 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.252 |
MOD_GlcNHglycan | 233 | 238 | PF01048 | 0.164 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.698 |
MOD_GlcNHglycan | 67 | 72 | PF01048 | 0.722 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.396 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.400 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.333 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.410 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.298 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.340 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.561 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.610 |
MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.368 |
MOD_N-GLC_1 | 355 | 360 | PF02516 | 0.634 |
MOD_N-GLC_2 | 64 | 66 | PF02516 | 0.752 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.317 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.246 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.396 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.596 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.633 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.406 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.365 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.346 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.303 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.608 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.403 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.319 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.351 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.524 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.420 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.728 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.500 |
MOD_SUMO_for_1 | 71 | 74 | PF00179 | 0.657 |
MOD_SUMO_rev_2 | 257 | 265 | PF00179 | 0.381 |
MOD_SUMO_rev_2 | 342 | 348 | PF00179 | 0.688 |
MOD_SUMO_rev_2 | 68 | 77 | PF00179 | 0.707 |
TRG_ENDOCYTIC_2 | 11 | 14 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.234 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.478 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZW5 | Leptomonas seymouri | 62% | 100% |
A0A0S4JCM6 | Bodo saltans | 25% | 100% |
A0A0S4JIE3 | Bodo saltans | 42% | 100% |
A0A1X0P7Q9 | Trypanosomatidae | 49% | 100% |
A0A3R7M9V1 | Trypanosoma rangeli | 47% | 100% |
A0A3S7XAT0 | Leishmania donovani | 88% | 99% |
A4HP62 | Leishmania braziliensis | 77% | 100% |
E9AG16 | Leishmania major | 90% | 100% |
E9AHX4 | Leishmania infantum | 86% | 100% |
Q8K0P3 | Mus musculus | 26% | 81% |
V5BGD9 | Trypanosoma cruzi | 47% | 100% |