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: E9AG16
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 | 356 | 360 | PF00656 | 0.702 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.322 |
DOC_ANK_TNKS_1 | 239 | 246 | PF00023 | 0.320 |
DOC_CKS1_1 | 68 | 73 | PF01111 | 0.591 |
DOC_MAPK_HePTP_8 | 163 | 175 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 166 | 175 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 361 | 369 | PF00069 | 0.607 |
DOC_PP2B_PxIxI_1 | 167 | 173 | PF00149 | 0.416 |
DOC_PP4_FxxP_1 | 311 | 314 | PF00568 | 0.287 |
DOC_PP4_FxxP_1 | 68 | 71 | PF00568 | 0.586 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.302 |
DOC_USP7_UBL2_3 | 86 | 90 | PF12436 | 0.550 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.503 |
LIG_14-3-3_CanoR_1 | 307 | 312 | PF00244 | 0.307 |
LIG_14-3-3_CanoR_1 | 315 | 324 | PF00244 | 0.306 |
LIG_Actin_WH2_2 | 329 | 344 | PF00022 | 0.476 |
LIG_APCC_ABBA_1 | 32 | 37 | PF00400 | 0.364 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.379 |
LIG_BIR_III_2 | 126 | 130 | PF00653 | 0.411 |
LIG_BRCT_BRCA1_1 | 226 | 230 | PF00533 | 0.293 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.454 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.306 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.357 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.397 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.692 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.449 |
LIG_GBD_Chelix_1 | 120 | 128 | PF00786 | 0.390 |
LIG_LIR_Apic_2 | 309 | 314 | PF02991 | 0.290 |
LIG_LIR_Apic_2 | 67 | 71 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 10 | 21 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 155 | 164 | PF02991 | 0.265 |
LIG_LIR_Gen_1 | 187 | 194 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 264 | 274 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 37 | 47 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 155 | 159 | PF02991 | 0.198 |
LIG_LIR_Nem_3 | 187 | 193 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 20 | 24 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 229 | 234 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 264 | 269 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 4 | 9 | PF02991 | 0.687 |
LIG_PDZ_Class_1 | 378 | 383 | PF00595 | 0.615 |
LIG_Pex14_1 | 143 | 147 | PF04695 | 0.313 |
LIG_Pex14_2 | 266 | 270 | PF04695 | 0.287 |
LIG_Pex14_2 | 293 | 297 | PF04695 | 0.287 |
LIG_SH2_CRK | 19 | 23 | PF00017 | 0.384 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.400 |
LIG_SH2_CRK | 92 | 96 | PF00017 | 0.570 |
LIG_SH2_PTP2 | 11 | 14 | PF00017 | 0.412 |
LIG_SH2_PTP2 | 21 | 24 | PF00017 | 0.369 |
LIG_SH2_PTP2 | 25 | 28 | PF00017 | 0.366 |
LIG_SH2_PTP2 | 35 | 38 | PF00017 | 0.372 |
LIG_SH2_SRC | 11 | 14 | PF00017 | 0.412 |
LIG_SH2_SRC | 21 | 24 | PF00017 | 0.369 |
LIG_SH2_SRC | 242 | 245 | PF00017 | 0.270 |
LIG_SH2_SRC | 25 | 28 | PF00017 | 0.366 |
LIG_SH2_SRC | 35 | 38 | PF00017 | 0.359 |
LIG_SH2_STAP1 | 147 | 151 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.374 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.677 |
LIG_SUMO_SIM_anti_2 | 169 | 174 | PF11976 | 0.287 |
LIG_SUMO_SIM_par_1 | 112 | 117 | PF11976 | 0.514 |
LIG_TRAF2_1 | 274 | 277 | PF00917 | 0.416 |
LIG_UBA3_1 | 170 | 176 | PF00899 | 0.416 |
LIG_WRC_WIRS_1 | 147 | 152 | PF05994 | 0.355 |
MOD_CDK_SPK_2 | 114 | 119 | PF00069 | 0.469 |
MOD_CDK_SPK_2 | 175 | 180 | PF00069 | 0.345 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.509 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.333 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.458 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.674 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.772 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.372 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.312 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.372 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.711 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.456 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.291 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.697 |
MOD_GlcNHglycan | 81 | 86 | PF01048 | 0.719 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.428 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.414 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.390 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.381 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.346 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.526 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.686 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.355 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.436 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.612 |
MOD_N-GLC_2 | 78 | 80 | PF02516 | 0.632 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.406 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.274 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.399 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.508 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.583 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.651 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.381 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.351 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.339 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.238 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.682 |
MOD_Plk_2-3 | 248 | 254 | PF00069 | 0.270 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.387 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.230 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.434 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.383 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.463 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.350 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.426 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.761 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.494 |
MOD_SUMO_rev_2 | 271 | 279 | PF00179 | 0.366 |
MOD_SUMO_rev_2 | 356 | 362 | PF00179 | 0.495 |
MOD_SUMO_rev_2 | 82 | 91 | PF00179 | 0.690 |
TRG_ENDOCYTIC_2 | 11 | 14 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 35 | 38 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.372 |
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 | 85% | 100% |
A4HP62 | Leishmania braziliensis | 78% | 100% |
E9AHX4 | Leishmania infantum | 89% | 100% |
E9ASX0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BGD9 | Trypanosoma cruzi | 47% | 100% |