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: 0, no: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
Related structures:
AlphaFold database: A0A3S7WXS2
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 20 |
GO:0008152 | metabolic process | 1 | 20 |
GO:0044238 | primary metabolic process | 2 | 20 |
GO:0071704 | organic substance metabolic process | 2 | 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 20 |
GO:0004553 | hydrolase activity, hydrolyzing O-glycosyl compounds | 4 | 20 |
GO:0004564 | beta-fructofuranosidase activity | 5 | 18 |
GO:0016787 | hydrolase activity | 2 | 20 |
GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 20 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.332 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.335 |
CLV_PCSK_PC1ET2_1 | 440 | 442 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.195 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.372 |
DEG_COP1_1 | 381 | 390 | PF00400 | 0.332 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.544 |
DOC_CDC14_PxL_1 | 384 | 392 | PF14671 | 0.325 |
DOC_CKS1_1 | 293 | 298 | PF01111 | 0.209 |
DOC_CKS1_1 | 379 | 384 | PF01111 | 0.390 |
DOC_MAPK_MEF2A_6 | 261 | 268 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 475 | 482 | PF00069 | 0.274 |
DOC_MAPK_NFAT4_5 | 261 | 269 | PF00069 | 0.253 |
DOC_PP1_RVXF_1 | 263 | 270 | PF00149 | 0.272 |
DOC_PP2B_LxvP_1 | 353 | 356 | PF13499 | 0.339 |
DOC_PP4_FxxP_1 | 192 | 195 | PF00568 | 0.339 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.427 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.231 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.387 |
LIG_14-3-3_CanoR_1 | 503 | 508 | PF00244 | 0.437 |
LIG_APCC_ABBA_1 | 469 | 474 | PF00400 | 0.299 |
LIG_BRCT_BRCA1_1 | 490 | 494 | PF00533 | 0.372 |
LIG_deltaCOP1_diTrp_1 | 85 | 92 | PF00928 | 0.309 |
LIG_DLG_GKlike_1 | 357 | 365 | PF00625 | 0.253 |
LIG_EH_1 | 80 | 84 | PF12763 | 0.322 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.390 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.300 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.318 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.290 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.265 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.272 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.318 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.324 |
LIG_KLC1_Yacidic_2 | 432 | 436 | PF13176 | 0.478 |
LIG_LIR_Gen_1 | 233 | 241 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 233 | 239 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 254 | 258 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 305 | 309 | PF02991 | 0.342 |
LIG_NRBOX | 216 | 222 | PF00104 | 0.384 |
LIG_Pex14_1 | 48 | 52 | PF04695 | 0.376 |
LIG_Pex14_2 | 83 | 87 | PF04695 | 0.269 |
LIG_PTB_Apo_2 | 128 | 135 | PF02174 | 0.297 |
LIG_PTB_Apo_2 | 442 | 449 | PF02174 | 0.335 |
LIG_PTB_Apo_2 | 68 | 75 | PF02174 | 0.272 |
LIG_PTB_Phospho_1 | 128 | 134 | PF10480 | 0.297 |
LIG_PTB_Phospho_1 | 442 | 448 | PF10480 | 0.335 |
LIG_PTB_Phospho_1 | 68 | 74 | PF10480 | 0.272 |
LIG_SH2_GRB2like | 69 | 72 | PF00017 | 0.272 |
LIG_SH2_NCK_1 | 361 | 365 | PF00017 | 0.272 |
LIG_SH2_SRC | 434 | 437 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 407 | 411 | PF00017 | 0.332 |
LIG_SH2_STAT3 | 162 | 165 | PF00017 | 0.318 |
LIG_SH2_STAT3 | 316 | 319 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.241 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.470 |
LIG_SH3_2 | 296 | 301 | PF14604 | 0.209 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.339 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.312 |
LIG_SUMO_SIM_par_1 | 388 | 393 | PF11976 | 0.273 |
LIG_TRAF2_1 | 25 | 28 | PF00917 | 0.385 |
LIG_WRC_WIRS_1 | 54 | 59 | PF05994 | 0.228 |
LIG_WW_1 | 186 | 189 | PF00397 | 0.384 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.291 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.208 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.272 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.518 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.253 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.332 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.335 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.335 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.335 |
MOD_Cter_Amidation | 272 | 275 | PF01082 | 0.272 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.328 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.475 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.315 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.408 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.523 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.372 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.335 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.247 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.549 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.334 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.347 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.335 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.316 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.345 |
MOD_N-GLC_1 | 393 | 398 | PF02516 | 0.272 |
MOD_N-GLC_1 | 402 | 407 | PF02516 | 0.235 |
MOD_N-GLC_1 | 507 | 512 | PF02516 | 0.422 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.339 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.358 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.509 |
MOD_PK_1 | 39 | 45 | PF00069 | 0.302 |
MOD_PK_1 | 503 | 509 | PF00069 | 0.307 |
MOD_PKA_1 | 274 | 280 | PF00069 | 0.272 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.299 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.422 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.382 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.253 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.361 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.335 |
MOD_Plk_1 | 485 | 491 | PF00069 | 0.335 |
MOD_Plk_2-3 | 474 | 480 | PF00069 | 0.335 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.297 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.422 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.277 |
MOD_Plk_4 | 514 | 520 | PF00069 | 0.409 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.231 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.384 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.390 |
MOD_SUMO_for_1 | 20 | 23 | PF00179 | 0.497 |
MOD_SUMO_rev_2 | 260 | 267 | PF00179 | 0.251 |
TRG_DiLeu_BaEn_1 | 262 | 267 | PF01217 | 0.253 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.339 |
TRG_ER_diArg_1 | 281 | 284 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 328 | 330 | PF00400 | 0.332 |
TRG_NES_CRM1_1 | 460 | 474 | PF08389 | 0.437 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8F7 | Leptomonas seymouri | 52% | 100% |
A0A0N1PBT6 | Leptomonas seymouri | 27% | 82% |
A0A1X0NFY9 | Trypanosomatidae | 26% | 100% |
A0A1X0NTL0 | Trypanosomatidae | 24% | 83% |
A0A1X0NTM3 | Trypanosomatidae | 25% | 83% |
A0A1X0NY19 | Trypanosomatidae | 28% | 83% |
A0A1X0P322 | Trypanosomatidae | 25% | 84% |
A0A1X0P5Y7 | Trypanosomatidae | 26% | 82% |
A0A3Q8IB13 | Leishmania donovani | 80% | 95% |
A0A3Q8IFU7 | Leishmania donovani | 100% | 100% |
A0A3S5H595 | Leishmania donovani | 27% | 82% |
A0A3S5H7I4 | Leishmania donovani | 52% | 98% |
A0A3S7WXQ4 | Leishmania donovani | 86% | 100% |
A1STJ9 | Psychromonas ingrahamii (strain 37) | 33% | 97% |
A2R0E0 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 25% | 98% |
A2X5P7 | Oryza sativa subsp. indica | 27% | 91% |
A2YZ01 | Oryza sativa subsp. indica | 30% | 88% |
A4H3V1 | Leishmania braziliensis | 28% | 82% |
A4HCV9 | Leishmania braziliensis | 69% | 99% |
A4HCW0 | Leishmania braziliensis | 78% | 99% |
A4HG14 | Leishmania braziliensis | 50% | 98% |
A4HS26 | Leishmania infantum | 27% | 82% |
A4I0D9 | Leishmania infantum | 80% | 99% |
A4I0E0 | Leishmania infantum | 86% | 100% |
A4I336 | Leishmania infantum | 51% | 98% |
A4IAW1 | Leishmania infantum | 27% | 75% |
A5ABL2 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 26% | 100% |
A5DHM6 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 26% | 100% |
A5EZZ8 | Vibrio cholerae serotype O1 (strain ATCC 39541 / Classical Ogawa 395 / O395) | 32% | 97% |
A8W7I5 | Meyerozyma guilliermondii | 26% | 100% |
B6DXP5 | Leymus chinensis | 26% | 88% |
B6DZC8 | Triticum aestivum | 25% | 88% |
B6DZD0 | Triticum urartu | 25% | 88% |
B6DZD1 | Aegilops speltoides | 25% | 89% |
B6DZD2 | Aegilops tauschii | 25% | 88% |
D2IGW7 | Bromus pictus | 25% | 88% |
E1ABX2 | Aspergillus ficuum | 26% | 98% |
E8NHF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 99% |
E8NHF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 99% |
E9ACV4 | Leishmania major | 52% | 98% |
E9AK13 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AWA3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
E9AZE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 97% |
F8DVG5 | Zymomonas mobilis subsp. mobilis (strain ATCC 10988 / DSM 424 / LMG 404 / NCIMB 8938 / NRRL B-806 / ZM1) | 39% | 100% |
H2DF87 | Rosa hybrid cultivar | 28% | 90% |
H2DF88 | Rosa hybrid cultivar | 26% | 82% |
K0E681 | Aspergillus rugulosus | 26% | 100% |
O07003 | Bacillus subtilis (strain 168) | 26% | 100% |
O33833 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 32% | 100% |
O42878 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
O59852 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 91% |
O74641 | Aspergillus niger | 26% | 100% |
O74642 | Aspergillus niger | 26% | 100% |
O94220 | Aspergillus ficuum | 26% | 100% |
P00724 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 99% |
P05656 | Bacillus subtilis (strain 168) | 28% | 78% |
P07819 | Bacillus subtilis (strain 168) | 35% | 100% |
P0DJA7 | Zymomonas mobilis subsp. mobilis (strain ATCC 31821 / ZM4 / CP4) | 39% | 100% |
P10594 | Saccharomyces cerevisiae | 24% | 99% |
P10596 | Saccharomyces cerevisiae | 23% | 99% |
P13394 | Vibrio alginolyticus | 30% | 100% |
P13522 | Streptococcus mutans serotype c (strain ATCC 700610 / UA159) | 29% | 100% |
P16553 | Escherichia coli | 46% | 100% |
P24133 | Schwanniomyces occidentalis | 24% | 99% |
P27217 | Klebsiella pneumoniae | 35% | 100% |
P28999 | Kluyveromyces marxianus | 25% | 95% |
P29000 | Solanum lycopersicum | 26% | 83% |
P29001 | Vigna radiata var. radiata | 26% | 81% |
P37075 | Salmonella typhimurium | 36% | 100% |
P40714 | Escherichia coli | 47% | 100% |
P40912 | Wickerhamomyces anomalus | 24% | 96% |
P43471 | Pediococcus pentosaceus | 26% | 100% |
P49174 | Zea mays | 26% | 89% |
P49175 | Zea mays | 26% | 79% |
P80065 | Daucus carota | 26% | 80% |
P92916 | Allium cepa | 24% | 86% |
P93761 | Capsicum annuum | 25% | 82% |
P94469 | Geobacillus stearothermophilus | 27% | 100% |
Q01IS7 | Oryza sativa subsp. indica | 25% | 88% |
Q01IS8 | Oryza sativa subsp. indica | 25% | 90% |
Q04937 | Lactococcus lactis subsp. lactis | 28% | 100% |
Q05936 | Staphylococcus xylosus | 30% | 100% |
Q0E0P0 | Oryza sativa subsp. japonica | 27% | 91% |
Q0J360 | Oryza sativa subsp. japonica | 25% | 88% |
Q0JDC5 | Oryza sativa subsp. japonica | 25% | 88% |
Q0JDC6 | Oryza sativa subsp. japonica | 25% | 90% |
Q1PEF8 | Arabidopsis thaliana | 26% | 89% |
Q2UXF7 | Triticum aestivum | 29% | 88% |
Q39692 | Daucus carota | 30% | 89% |
Q39693 | Daucus carota | 30% | 90% |
Q43089 | Pisum sativum | 25% | 95% |
Q43348 | Arabidopsis thaliana | 24% | 81% |
Q43857 | Vicia faba | 25% | 82% |
Q43866 | Arabidopsis thaliana | 26% | 90% |
Q4QB75 | Leishmania major | 84% | 100% |
Q4QB76 | Leishmania major | 78% | 99% |
Q56660 | Vibrio cholerae | 31% | 97% |
Q56UD0 | Oryza sativa subsp. japonica | 28% | 88% |
Q56UD1 | Oryza sativa subsp. japonica | 24% | 97% |
Q5FC15 | Asparagus officinalis | 25% | 86% |
Q5JJV0 | Oryza sativa subsp. japonica | 27% | 89% |
Q67XZ3 | Arabidopsis thaliana | 28% | 89% |
Q70AT7 | Hordeum vulgare | 26% | 88% |
Q70XE6 | Beta vulgaris | 27% | 87% |
Q76HP6 | Aspergillus niger | 26% | 98% |
Q84LA1 | Triticum aestivum | 25% | 88% |
Q84PN8 | Triticum aestivum | 25% | 88% |
Q8W413 | Arabidopsis thaliana | 28% | 89% |
Q8W4S6 | Arabidopsis thaliana | 24% | 96% |
Q96TU3 | Aspergillus awamori | 25% | 98% |
Q9FSV7 | Festuca arundinacea | 24% | 81% |
Q9KLT6 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 30% | 96% |
Q9LIB9 | Arabidopsis thaliana | 23% | 92% |
Q9XTP3 | Leishmania major | 26% | 82% |