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 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A4HCV9
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_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.258 |
CLV_C14_Caspase3-7 | 343 | 347 | PF00656 | 0.193 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.295 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.262 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.321 |
CLV_PCSK_PC1ET2_1 | 40 | 42 | PF00082 | 0.246 |
CLV_PCSK_PC1ET2_1 | 459 | 461 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.201 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.369 |
DOC_ANK_TNKS_1 | 307 | 314 | PF00023 | 0.193 |
DOC_CYCLIN_RxL_1 | 374 | 385 | PF00134 | 0.290 |
DOC_CYCLIN_yCln2_LP_2 | 289 | 295 | PF00134 | 0.193 |
DOC_MAPK_MEF2A_6 | 494 | 501 | PF00069 | 0.283 |
DOC_PP2B_LxvP_1 | 373 | 376 | PF13499 | 0.320 |
DOC_PP4_FxxP_1 | 186 | 189 | PF00568 | 0.320 |
DOC_PP4_FxxP_1 | 336 | 339 | PF00568 | 0.278 |
DOC_PP4_MxPP_1 | 390 | 393 | PF00568 | 0.330 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.196 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.377 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.290 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.343 |
LIG_14-3-3_CanoR_1 | 316 | 322 | PF00244 | 0.263 |
LIG_14-3-3_CanoR_1 | 522 | 527 | PF00244 | 0.385 |
LIG_APCC_ABBA_1 | 488 | 493 | PF00400 | 0.283 |
LIG_BRCT_BRCA1_1 | 509 | 513 | PF00533 | 0.333 |
LIG_deltaCOP1_diTrp_1 | 79 | 86 | PF00928 | 0.292 |
LIG_EH_1 | 74 | 78 | PF12763 | 0.293 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.307 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.372 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.283 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.312 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.400 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.290 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.353 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.288 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.218 |
LIG_FHA_2 | 422 | 428 | PF00498 | 0.308 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.306 |
LIG_KLC1_Yacidic_2 | 451 | 455 | PF13176 | 0.418 |
LIG_LIR_Apic_2 | 335 | 339 | PF02991 | 0.278 |
LIG_LIR_Apic_2 | 356 | 361 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 227 | 235 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 248 | 252 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 324 | 330 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.318 |
LIG_NRBOX | 210 | 216 | PF00104 | 0.343 |
LIG_Pex14_1 | 317 | 321 | PF04695 | 0.263 |
LIG_Pex14_1 | 42 | 46 | PF04695 | 0.341 |
LIG_Pex14_2 | 77 | 81 | PF04695 | 0.289 |
LIG_PTB_Apo_2 | 122 | 129 | PF02174 | 0.273 |
LIG_PTB_Apo_2 | 461 | 468 | PF02174 | 0.317 |
LIG_PTB_Phospho_1 | 122 | 128 | PF10480 | 0.273 |
LIG_PTB_Phospho_1 | 461 | 467 | PF10480 | 0.317 |
LIG_RPA_C_Fungi | 270 | 282 | PF08784 | 0.263 |
LIG_SH2_GRB2like | 123 | 126 | PF00017 | 0.193 |
LIG_SH2_GRB2like | 270 | 273 | PF00017 | 0.218 |
LIG_SH2_GRB2like | 96 | 99 | PF00017 | 0.193 |
LIG_SH2_SRC | 453 | 456 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 123 | 127 | PF00017 | 0.254 |
LIG_SH2_STAP1 | 426 | 430 | PF00017 | 0.313 |
LIG_SH2_STAT3 | 156 | 159 | PF00017 | 0.300 |
LIG_SH2_STAT3 | 260 | 263 | PF00017 | 0.263 |
LIG_SH2_STAT3 | 337 | 340 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.463 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.320 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.193 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.265 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.218 |
LIG_WRC_WIRS_1 | 318 | 323 | PF05994 | 0.263 |
LIG_WW_1 | 180 | 183 | PF00397 | 0.343 |
MOD_CDK_SPK_2 | 3 | 8 | PF00069 | 0.460 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.275 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.258 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.262 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.474 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.239 |
MOD_CK2_1 | 421 | 427 | PF00069 | 0.324 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.362 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.333 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.321 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.508 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.310 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.364 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.263 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.362 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.333 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.317 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.257 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.511 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.303 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.197 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.316 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.328 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.255 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.257 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.317 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.361 |
MOD_N-GLC_1 | 27 | 32 | PF02516 | 0.329 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.320 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.225 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.290 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.346 |
MOD_NEK2_1 | 540 | 545 | PF00069 | 0.512 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.208 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.263 |
MOD_PK_1 | 522 | 528 | PF00069 | 0.290 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.283 |
MOD_PKB_1 | 273 | 281 | PF00069 | 0.290 |
MOD_Plk_1 | 27 | 33 | PF00069 | 0.349 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.269 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.343 |
MOD_Plk_1 | 492 | 498 | PF00069 | 0.317 |
MOD_Plk_1 | 504 | 510 | PF00069 | 0.317 |
MOD_Plk_1 | 540 | 546 | PF00069 | 0.365 |
MOD_Plk_2-3 | 493 | 499 | PF00069 | 0.317 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.273 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.273 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.263 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.365 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.290 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.465 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.343 |
MOD_SUMO_for_1 | 297 | 300 | PF00179 | 0.193 |
MOD_SUMO_rev_2 | 119 | 127 | PF00179 | 0.205 |
TRG_DiLeu_BaLyEn_6 | 414 | 419 | PF01217 | 0.341 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.334 |
TRG_ER_diArg_1 | 273 | 276 | PF00400 | 0.321 |
TRG_NES_CRM1_1 | 479 | 493 | PF08389 | 0.385 |
TRG_Pf-PMV_PEXEL_1 | 377 | 382 | PF00026 | 0.290 |
TRG_Pf-PMV_PEXEL_1 | 417 | 421 | PF00026 | 0.291 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8F7 | Leptomonas seymouri | 50% | 100% |
A0A0N1PBT6 | Leptomonas seymouri | 25% | 85% |
A0A1X0NFY9 | Trypanosomatidae | 24% | 100% |
A0A1X0NTL0 | Trypanosomatidae | 23% | 86% |
A0A1X0NTM3 | Trypanosomatidae | 24% | 86% |
A0A1X0NY19 | Trypanosomatidae | 26% | 86% |
A0A1X0P322 | Trypanosomatidae | 23% | 87% |
A0A1X0P5Y7 | Trypanosomatidae | 25% | 85% |
A0A3Q8IB13 | Leishmania donovani | 82% | 99% |
A0A3Q8IFU7 | Leishmania donovani | 69% | 100% |
A0A3S5H595 | Leishmania donovani | 24% | 85% |
A0A3S5H7I4 | Leishmania donovani | 49% | 100% |
A0A3S7WXQ4 | Leishmania donovani | 64% | 100% |
A0A3S7WXS2 | Leishmania donovani | 69% | 100% |
A1STJ9 | Psychromonas ingrahamii (strain 37) | 32% | 100% |
A2R0E0 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 26% | 100% |
A2X5P7 | Oryza sativa subsp. indica | 26% | 95% |
A2YZ01 | Oryza sativa subsp. indica | 24% | 92% |
A4H3V1 | Leishmania braziliensis | 24% | 85% |
A4HCW0 | Leishmania braziliensis | 68% | 93% |
A4HG14 | Leishmania braziliensis | 48% | 93% |
A4HS26 | Leishmania infantum | 24% | 85% |
A4I0D9 | Leishmania infantum | 82% | 99% |
A4I0E0 | Leishmania infantum | 64% | 100% |
A4I336 | Leishmania infantum | 49% | 100% |
A4IAW1 | Leishmania infantum | 25% | 78% |
A5ABL2 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 25% | 100% |
A5DHM6 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 25% | 100% |
A5EZZ8 | Vibrio cholerae serotype O1 (strain ATCC 39541 / Classical Ogawa 395 / O395) | 30% | 100% |
A8W7I5 | Meyerozyma guilliermondii | 24% | 100% |
B6DXP5 | Leymus chinensis | 24% | 91% |
B6DZC8 | Triticum aestivum | 23% | 92% |
B6DZD0 | Triticum urartu | 25% | 91% |
B6DZD1 | Aegilops speltoides | 24% | 92% |
B6DZD2 | Aegilops tauschii | 25% | 92% |
D2IGW7 | Bromus pictus | 24% | 91% |
E1ABX2 | Aspergillus ficuum | 26% | 100% |
E8NHF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
E8NHF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
E9ACV4 | Leishmania major | 50% | 93% |
E9AK13 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 86% |
E9AWA3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
E9AZE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
F8DVG5 | Zymomonas mobilis subsp. mobilis (strain ATCC 10988 / DSM 424 / LMG 404 / NCIMB 8938 / NRRL B-806 / ZM1) | 39% | 100% |
H2DF87 | Rosa hybrid cultivar | 26% | 93% |
H2DF88 | Rosa hybrid cultivar | 24% | 85% |
K0E681 | Aspergillus rugulosus | 25% | 100% |
O07003 | Bacillus subtilis (strain 168) | 24% | 100% |
O24509 | Phaseolus vulgaris | 26% | 84% |
O33833 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 31% | 100% |
O42878 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
O59852 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 94% |
O74641 | Aspergillus niger | 25% | 100% |
O74642 | Aspergillus niger | 25% | 100% |
O94220 | Aspergillus ficuum | 25% | 100% |
P00724 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
P05656 | Bacillus subtilis (strain 168) | 28% | 81% |
P07819 | Bacillus subtilis (strain 168) | 35% | 100% |
P0DJA7 | Zymomonas mobilis subsp. mobilis (strain ATCC 31821 / ZM4 / CP4) | 38% | 100% |
P10594 | Saccharomyces cerevisiae | 22% | 100% |
P10596 | Saccharomyces cerevisiae | 22% | 100% |
P13394 | Vibrio alginolyticus | 28% | 100% |
P13522 | Streptococcus mutans serotype c (strain ATCC 700610 / UA159) | 26% | 100% |
P16553 | Escherichia coli | 44% | 100% |
P26792 | Daucus carota | 26% | 92% |
P27217 | Klebsiella pneumoniae | 34% | 100% |
P29000 | Solanum lycopersicum | 24% | 86% |
P29001 | Vigna radiata var. radiata | 26% | 84% |
P37075 | Salmonella typhimurium | 32% | 100% |
P40714 | Escherichia coli | 43% | 100% |
P40912 | Wickerhamomyces anomalus | 22% | 99% |
P43471 | Pediococcus pentosaceus | 24% | 100% |
P49174 | Zea mays | 24% | 93% |
P49175 | Zea mays | 24% | 81% |
P80065 | Daucus carota | 26% | 83% |
P92916 | Allium cepa | 24% | 89% |
P93761 | Capsicum annuum | 25% | 85% |
P94469 | Geobacillus stearothermophilus | 24% | 100% |
Q01IS7 | Oryza sativa subsp. indica | 23% | 91% |
Q04937 | Lactococcus lactis subsp. lactis | 24% | 100% |
Q05936 | Staphylococcus xylosus | 29% | 100% |
Q0E0P0 | Oryza sativa subsp. japonica | 26% | 95% |
Q0J360 | Oryza sativa subsp. japonica | 24% | 92% |
Q0JDC5 | Oryza sativa subsp. japonica | 23% | 91% |
Q1PEF8 | Arabidopsis thaliana | 26% | 93% |
Q2UXF7 | Triticum aestivum | 23% | 91% |
Q39041 | Arabidopsis thaliana | 26% | 82% |
Q39692 | Daucus carota | 27% | 92% |
Q39693 | Daucus carota | 27% | 94% |
Q43089 | Pisum sativum | 23% | 98% |
Q43348 | Arabidopsis thaliana | 27% | 84% |
Q43857 | Vicia faba | 23% | 85% |
Q43866 | Arabidopsis thaliana | 26% | 93% |
Q4QB75 | Leishmania major | 62% | 96% |
Q4QB76 | Leishmania major | 82% | 100% |
Q56660 | Vibrio cholerae | 30% | 100% |
Q56UD0 | Oryza sativa subsp. japonica | 25% | 92% |
Q56UD1 | Oryza sativa subsp. japonica | 22% | 100% |
Q5FC15 | Asparagus officinalis | 25% | 90% |
Q5JJV0 | Oryza sativa subsp. japonica | 23% | 93% |
Q67XZ3 | Arabidopsis thaliana | 26% | 92% |
Q6BJW6 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 23% | 100% |
Q70AT7 | Hordeum vulgare | 24% | 91% |
Q70XE6 | Beta vulgaris | 25% | 90% |
Q76HP6 | Aspergillus niger | 26% | 100% |
Q84LA1 | Triticum aestivum | 25% | 92% |
Q84PN8 | Triticum aestivum | 25% | 91% |
Q8W413 | Arabidopsis thaliana | 25% | 92% |
Q8W4S6 | Arabidopsis thaliana | 25% | 99% |
Q96TU3 | Aspergillus awamori | 25% | 100% |
Q9FSV7 | Festuca arundinacea | 23% | 83% |
Q9KLT6 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 30% | 100% |
Q9LIB9 | Arabidopsis thaliana | 25% | 95% |
Q9XTP3 | Leishmania major | 24% | 85% |
Q9Y746 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 21% | 90% |