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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0016020 | membrane | 2 | 3 |
Related structures:
AlphaFold database: A4HC08
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016491 | oxidoreductase activity | 2 | 12 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0008812 | choline dehydrogenase activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.352 |
CLV_PCSK_FUR_1 | 154 | 158 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.426 |
CLV_PCSK_PC1ET2_1 | 156 | 158 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.720 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.275 |
DEG_APCC_DBOX_1 | 219 | 227 | PF00400 | 0.406 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.690 |
DOC_CKS1_1 | 101 | 106 | PF01111 | 0.321 |
DOC_CKS1_1 | 84 | 89 | PF01111 | 0.363 |
DOC_CYCLIN_RxL_1 | 217 | 225 | PF00134 | 0.426 |
DOC_CYCLIN_yCln2_LP_2 | 228 | 234 | PF00134 | 0.292 |
DOC_MAPK_DCC_7 | 301 | 311 | PF00069 | 0.216 |
DOC_MAPK_gen_1 | 140 | 149 | PF00069 | 0.363 |
DOC_MAPK_gen_1 | 474 | 483 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 142 | 151 | PF00069 | 0.426 |
DOC_PP1_RVXF_1 | 329 | 335 | PF00149 | 0.433 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.453 |
DOC_USP7_UBL2_3 | 511 | 515 | PF12436 | 0.402 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.328 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.340 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.308 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.345 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.340 |
LIG_14-3-3_CanoR_1 | 140 | 145 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 284 | 293 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 3 | 9 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 341 | 347 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 402 | 411 | PF00244 | 0.392 |
LIG_BRCT_BRCA1_1 | 16 | 20 | PF00533 | 0.506 |
LIG_BRCT_BRCA1_1 | 168 | 172 | PF00533 | 0.321 |
LIG_Clathr_ClatBox_1 | 265 | 269 | PF01394 | 0.453 |
LIG_CSL_BTD_1 | 99 | 102 | PF09270 | 0.426 |
LIG_deltaCOP1_diTrp_1 | 122 | 133 | PF00928 | 0.317 |
LIG_eIF4E_1 | 431 | 437 | PF01652 | 0.426 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.321 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.303 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.287 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.359 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.380 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.351 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.422 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.681 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.416 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.321 |
LIG_LIR_Gen_1 | 143 | 152 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 17 | 25 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 348 | 356 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 59 | 69 | PF02991 | 0.453 |
LIG_LIR_LC3C_4 | 269 | 274 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 348 | 353 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 440 | 445 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.426 |
LIG_MLH1_MIPbox_1 | 168 | 172 | PF16413 | 0.340 |
LIG_PCNA_yPIPBox_3 | 215 | 227 | PF02747 | 0.399 |
LIG_Pex14_2 | 168 | 172 | PF04695 | 0.372 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.392 |
LIG_SH2_SRC | 324 | 327 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 500 | 504 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.122 |
LIG_SH3_1 | 438 | 444 | PF00018 | 0.453 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.363 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.451 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.453 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.312 |
LIG_SUMO_SIM_anti_2 | 21 | 26 | PF11976 | 0.426 |
LIG_SUMO_SIM_anti_2 | 269 | 276 | PF11976 | 0.453 |
LIG_SUMO_SIM_anti_2 | 421 | 426 | PF11976 | 0.180 |
LIG_SUMO_SIM_par_1 | 264 | 271 | PF11976 | 0.426 |
LIG_SUMO_SIM_par_1 | 44 | 50 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 500 | 506 | PF11976 | 0.340 |
LIG_TRAF2_2 | 87 | 92 | PF00917 | 0.426 |
LIG_UBA3_1 | 222 | 227 | PF00899 | 0.340 |
LIG_WRC_WIRS_1 | 141 | 146 | PF05994 | 0.426 |
MOD_CDK_SPK_2 | 100 | 105 | PF00069 | 0.340 |
MOD_CDK_SPxxK_3 | 166 | 173 | PF00069 | 0.320 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.453 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.200 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.349 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.373 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.303 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.441 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.404 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.363 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.441 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.469 |
MOD_Cter_Amidation | 154 | 157 | PF01082 | 0.340 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.350 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.439 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.391 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.454 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.354 |
MOD_GlcNHglycan | 455 | 459 | PF01048 | 0.309 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.312 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.444 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.310 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.416 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.353 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.313 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.382 |
MOD_LATS_1 | 451 | 457 | PF00433 | 0.355 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.409 |
MOD_N-GLC_1 | 214 | 219 | PF02516 | 0.391 |
MOD_N-GLC_1 | 295 | 300 | PF02516 | 0.247 |
MOD_N-GLC_1 | 407 | 412 | PF02516 | 0.453 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.363 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.322 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.447 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.391 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.331 |
MOD_NEK2_2 | 254 | 259 | PF00069 | 0.453 |
MOD_NEK2_2 | 342 | 347 | PF00069 | 0.478 |
MOD_PIKK_1 | 177 | 183 | PF00454 | 0.426 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.502 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.287 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.411 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.468 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.499 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.484 |
MOD_PKA_2 | 528 | 534 | PF00069 | 0.469 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.411 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.361 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.426 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.457 |
MOD_Plk_1 | 484 | 490 | PF00069 | 0.321 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.319 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.367 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.389 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.200 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.265 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.317 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.328 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.340 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.308 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.400 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.454 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.345 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.340 |
TRG_DiLeu_BaLyEn_6 | 281 | 286 | PF01217 | 0.322 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.426 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.688 |
TRG_ER_diArg_1 | 139 | 142 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 258 | 260 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.507 |
TRG_NLS_MonoExtN_4 | 154 | 160 | PF00514 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUY3 | Leptomonas seymouri | 75% | 100% |
A0A0S4JLI4 | Bodo saltans | 41% | 93% |
A0A1X0NHH3 | Trypanosomatidae | 48% | 100% |
A0A3Q8IC21 | Leishmania donovani | 90% | 100% |
A0A3R7KBI5 | Trypanosoma rangeli | 48% | 100% |
A4HZM3 | Leishmania infantum | 90% | 100% |
A5IW37 | Staphylococcus aureus (strain JH9) | 23% | 94% |
A6QK99 | Staphylococcus aureus (strain Newman) | 23% | 94% |
A6U4Z2 | Staphylococcus aureus (strain JH1) | 23% | 94% |
A6U6Y8 | Sinorhizobium medicae (strain WSM419) | 23% | 97% |
A6X2G7 | Brucella anthropi (strain ATCC 49188 / DSM 6882 / CCUG 24695 / JCM 21032 / LMG 3331 / NBRC 15819 / NCTC 12168 / Alc 37) | 25% | 97% |
A7N2P9 | Vibrio campbellii (strain ATCC BAA-1116) | 25% | 94% |
A7X6Z3 | Staphylococcus aureus (strain Mu3 / ATCC 700698) | 23% | 94% |
A8Z5A4 | Staphylococcus aureus (strain USA300 / TCH1516) | 23% | 94% |
C3MIE4 | Sinorhizobium fredii (strain NBRC 101917 / NGR234) | 23% | 97% |
D0A120 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9AVE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
P60336 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 23% | 94% |
P60337 | Staphylococcus aureus (strain N315) | 23% | 94% |
Q2FDP9 | Staphylococcus aureus (strain USA300) | 23% | 94% |
Q2FV11 | Staphylococcus aureus (strain NCTC 8325 / PS 47) | 23% | 94% |
Q2YWJ5 | Staphylococcus aureus (strain bovine RF122 / ET3-1) | 23% | 94% |
Q47944 | Gluconobacter oxydans | 23% | 100% |
Q4A0Q1 | Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM 20229 / NCIMB 8711 / NCTC 7292 / S-41) | 24% | 96% |
Q4L9D7 | Staphylococcus haemolyticus (strain JCSC1435) | 24% | 94% |
Q4QC34 | Leishmania major | 89% | 100% |
Q5HCU1 | Staphylococcus aureus (strain COL) | 23% | 94% |
Q6G664 | Staphylococcus aureus (strain MSSA476) | 23% | 94% |
Q6GDJ1 | Staphylococcus aureus (strain MRSA252) | 23% | 94% |
Q7MF12 | Vibrio vulnificus (strain YJ016) | 23% | 96% |
Q8D3K2 | Vibrio vulnificus (strain CMCP6) | 24% | 96% |
Q8NUM0 | Staphylococcus aureus (strain MW2) | 23% | 94% |
Q985M5 | Mesorhizobium japonicum (strain LMG 29417 / CECT 9101 / MAFF 303099) | 23% | 97% |
Q9X2M2 | Staphylococcus xylosus | 24% | 96% |
V5DIB3 | Trypanosoma cruzi | 48% | 100% |