Despite the signature matches, it is both structurally and sequence-wise very dissimilar from rhomboids.
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 | yes | yes: 5, no: 5 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: E9AJK6
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 3 |
GO:0006066 | alcohol metabolic process | 3 | 3 |
GO:0006071 | glycerol metabolic process | 5 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0019400 | alditol metabolic process | 4 | 3 |
GO:0019751 | polyol metabolic process | 4 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 3 |
GO:0044281 | small molecule metabolic process | 2 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004371 | glycerone kinase activity | 5 | 3 |
GO:0016301 | kinase activity | 4 | 3 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 3 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 3 |
GO:0004175 | endopeptidase activity | 4 | 4 |
GO:0004252 | serine-type endopeptidase activity | 5 | 4 |
GO:0008233 | peptidase activity | 3 | 4 |
GO:0008236 | serine-type peptidase activity | 4 | 4 |
GO:0016787 | hydrolase activity | 2 | 4 |
GO:0017171 | serine hydrolase activity | 3 | 4 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 194 | 198 | PF00656 | 0.494 |
CLV_C14_Caspase3-7 | 228 | 232 | PF00656 | 0.443 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.743 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.745 |
CLV_PCSK_PC1ET2_1 | 51 | 53 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.537 |
DOC_CDC14_PxL_1 | 11 | 19 | PF14671 | 0.394 |
DOC_CYCLIN_RxL_1 | 337 | 347 | PF00134 | 0.383 |
DOC_MAPK_gen_1 | 337 | 344 | PF00069 | 0.376 |
DOC_MAPK_gen_1 | 38 | 48 | PF00069 | 0.382 |
DOC_MAPK_gen_1 | 51 | 62 | PF00069 | 0.282 |
DOC_MAPK_MEF2A_6 | 357 | 366 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 55 | 64 | PF00069 | 0.316 |
DOC_PP2B_LxvP_1 | 263 | 266 | PF13499 | 0.596 |
DOC_PP2B_LxvP_1 | 282 | 285 | PF13499 | 0.466 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.682 |
LIG_14-3-3_CanoR_1 | 122 | 131 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 256 | 265 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 299 | 309 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 341 | 351 | PF00244 | 0.281 |
LIG_14-3-3_CanoR_1 | 41 | 47 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 55 | 64 | PF00244 | 0.352 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.571 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.686 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.642 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.438 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.310 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.417 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.538 |
LIG_LIR_Gen_1 | 259 | 269 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 360 | 370 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 58 | 69 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 259 | 264 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.684 |
LIG_LIR_Nem_3 | 360 | 366 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 82 | 86 | PF02991 | 0.374 |
LIG_PDZ_Class_1 | 365 | 370 | PF00595 | 0.514 |
LIG_Pex14_1 | 327 | 331 | PF04695 | 0.181 |
LIG_Pex14_2 | 323 | 327 | PF04695 | 0.181 |
LIG_RPA_C_Fungi | 169 | 181 | PF08784 | 0.499 |
LIG_SH2_PTP2 | 279 | 282 | PF00017 | 0.512 |
LIG_SH2_PTP2 | 363 | 366 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 292 | 296 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.516 |
LIG_Sin3_3 | 261 | 268 | PF02671 | 0.432 |
LIG_SUMO_SIM_par_1 | 15 | 21 | PF11976 | 0.415 |
LIG_TRAF2_1 | 225 | 228 | PF00917 | 0.510 |
LIG_UBA3_1 | 200 | 206 | PF00899 | 0.491 |
LIG_WRC_WIRS_1 | 73 | 78 | PF05994 | 0.487 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.421 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.474 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.515 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.366 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.500 |
MOD_GlcNHglycan | 105 | 111 | PF01048 | 0.595 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.505 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.450 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.452 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.503 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.268 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.338 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.548 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.431 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.486 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.477 |
MOD_LATS_1 | 254 | 260 | PF00433 | 0.266 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.449 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.536 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.662 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.541 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.362 |
MOD_PIKK_1 | 158 | 164 | PF00454 | 0.181 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.536 |
MOD_PIKK_1 | 342 | 348 | PF00454 | 0.324 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.370 |
MOD_PKA_1 | 97 | 103 | PF00069 | 0.621 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.278 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.721 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.446 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 363 | 366 | PF00928 | 0.420 |
TRG_ER_diArg_1 | 134 | 137 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 172 | 174 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 211 | 214 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 340 | 343 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 348 | 350 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 364 | 367 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.627 |
TRG_NLS_MonoExtC_3 | 336 | 341 | PF00514 | 0.538 |
TRG_PTS1 | 367 | 370 | PF00515 | 0.566 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IG61 | Leptomonas seymouri | 54% | 100% |
A0A1X0NK02 | Trypanosomatidae | 33% | 100% |
A0A3R7KGS4 | Trypanosoma rangeli | 30% | 100% |
A0A3S5H501 | Leishmania donovani | 85% | 100% |
A4H3C4 | Leishmania braziliensis | 65% | 100% |
A4HRP0 | Leishmania infantum | 85% | 100% |
C9ZJ23 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9ACB8 | Leishmania major | 84% | 100% |
V5BCY2 | Trypanosoma cruzi | 30% | 71% |