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: Q4QB75
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 | 142 | 146 | PF00656 | 0.278 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.415 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.394 |
CLV_PCSK_PC1ET2_1 | 426 | 428 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.195 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.371 |
DEG_COP1_1 | 367 | 376 | PF00400 | 0.329 |
DOC_CDC14_PxL_1 | 370 | 378 | PF14671 | 0.323 |
DOC_CKS1_1 | 365 | 370 | PF01111 | 0.446 |
DOC_MAPK_MEF2A_6 | 247 | 254 | PF00069 | 0.322 |
DOC_MAPK_MEF2A_6 | 443 | 451 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 461 | 468 | PF00069 | 0.329 |
DOC_MAPK_NFAT4_5 | 247 | 255 | PF00069 | 0.252 |
DOC_PP1_RVXF_1 | 249 | 256 | PF00149 | 0.271 |
DOC_PP2B_LxvP_1 | 339 | 342 | PF13499 | 0.397 |
DOC_PP4_FxxP_1 | 178 | 181 | PF00568 | 0.397 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.227 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.407 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.240 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.443 |
LIG_14-3-3_CanoR_1 | 489 | 494 | PF00244 | 0.436 |
LIG_APCC_ABBA_1 | 455 | 460 | PF00400 | 0.358 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.760 |
LIG_BRCT_BRCA1_1 | 476 | 480 | PF00533 | 0.371 |
LIG_deltaCOP1_diTrp_1 | 79 | 85 | PF00928 | 0.363 |
LIG_DLG_GKlike_1 | 343 | 351 | PF00625 | 0.252 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.240 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.440 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.358 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.377 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.246 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.384 |
LIG_FHA_2 | 208 | 214 | PF00498 | 0.315 |
LIG_FHA_2 | 389 | 395 | PF00498 | 0.377 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.383 |
LIG_KLC1_Yacidic_2 | 418 | 422 | PF13176 | 0.477 |
LIG_LIR_Gen_1 | 219 | 227 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 65 | 75 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 124 | 130 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 187 | 193 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 240 | 244 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 291 | 295 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 65 | 70 | PF02991 | 0.267 |
LIG_NRBOX | 202 | 208 | PF00104 | 0.384 |
LIG_Pex14_1 | 41 | 45 | PF04695 | 0.390 |
LIG_PTB_Apo_2 | 428 | 435 | PF02174 | 0.394 |
LIG_PTB_Phospho_1 | 428 | 434 | PF10480 | 0.394 |
LIG_SH2_NCK_1 | 347 | 351 | PF00017 | 0.271 |
LIG_SH2_SRC | 420 | 423 | PF00017 | 0.481 |
LIG_SH2_SRC | 71 | 74 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 393 | 397 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 76 | 80 | PF00017 | 0.259 |
LIG_SH2_STAT3 | 302 | 305 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.240 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.494 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.259 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.338 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.311 |
LIG_TRFH_1 | 45 | 49 | PF08558 | 0.233 |
LIG_WW_1 | 172 | 175 | PF00397 | 0.384 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.550 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.252 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.391 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.394 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.394 |
MOD_CK2_1 | 459 | 465 | PF00069 | 0.394 |
MOD_Cter_Amidation | 258 | 261 | PF01082 | 0.271 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.387 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.407 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.371 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.393 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.259 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.392 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.414 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.406 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.394 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.375 |
MOD_N-GLC_1 | 37 | 42 | PF02516 | 0.367 |
MOD_N-GLC_1 | 379 | 384 | PF02516 | 0.352 |
MOD_N-GLC_1 | 388 | 393 | PF02516 | 0.235 |
MOD_N-GLC_1 | 493 | 498 | PF02516 | 0.421 |
MOD_N-GLC_2 | 112 | 114 | PF02516 | 0.202 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.338 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.425 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.519 |
MOD_PK_1 | 489 | 495 | PF00069 | 0.366 |
MOD_PKA_1 | 260 | 266 | PF00069 | 0.271 |
MOD_PKA_1 | 32 | 38 | PF00069 | 0.329 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.442 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.433 |
MOD_PKA_2 | 460 | 466 | PF00069 | 0.358 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.252 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.365 |
MOD_Plk_1 | 388 | 394 | PF00069 | 0.417 |
MOD_Plk_1 | 459 | 465 | PF00069 | 0.394 |
MOD_Plk_1 | 471 | 477 | PF00069 | 0.394 |
MOD_Plk_2-3 | 460 | 466 | PF00069 | 0.394 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.498 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.361 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.453 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.240 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.384 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.446 |
MOD_SUMO_rev_2 | 246 | 253 | PF00179 | 0.250 |
TRG_DiLeu_BaEn_1 | 248 | 253 | PF01217 | 0.252 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.397 |
TRG_ER_diArg_1 | 267 | 270 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 314 | 316 | PF00400 | 0.390 |
TRG_NES_CRM1_1 | 446 | 460 | PF08389 | 0.436 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8F7 | Leptomonas seymouri | 52% | 100% |
A0A0N1PBT6 | Leptomonas seymouri | 27% | 80% |
A0A1X0NFY9 | Trypanosomatidae | 27% | 100% |
A0A1X0NTL0 | Trypanosomatidae | 26% | 81% |
A0A1X0NTM3 | Trypanosomatidae | 27% | 81% |
A0A1X0NY19 | Trypanosomatidae | 28% | 81% |
A0A1X0P322 | Trypanosomatidae | 26% | 81% |
A0A1X0P5Y7 | Trypanosomatidae | 26% | 80% |
A0A3Q8IB13 | Leishmania donovani | 65% | 93% |
A0A3Q8IFU7 | Leishmania donovani | 84% | 97% |
A0A3S5H595 | Leishmania donovani | 27% | 80% |
A0A3S5H7I4 | Leishmania donovani | 51% | 100% |
A0A3S7WXQ4 | Leishmania donovani | 96% | 100% |
A0A3S7WXS2 | Leishmania donovani | 84% | 97% |
A1STJ9 | Psychromonas ingrahamii (strain 37) | 34% | 94% |
A2R0E0 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 25% | 96% |
A2X5P7 | Oryza sativa subsp. indica | 28% | 89% |
A2YZ01 | Oryza sativa subsp. indica | 28% | 86% |
A4H3V1 | Leishmania braziliensis | 27% | 80% |
A4HCV9 | Leishmania braziliensis | 62% | 94% |
A4HCW0 | Leishmania braziliensis | 85% | 100% |
A4HG14 | Leishmania braziliensis | 51% | 100% |
A4HS26 | Leishmania infantum | 27% | 80% |
A4I0D9 | Leishmania infantum | 65% | 93% |
A4I0E0 | Leishmania infantum | 96% | 100% |
A4I336 | Leishmania infantum | 51% | 100% |
A4IAW1 | Leishmania infantum | 28% | 73% |
A5ABL2 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 25% | 99% |
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% | 94% |
A8W7I5 | Meyerozyma guilliermondii | 26% | 100% |
B6DXP5 | Leymus chinensis | 25% | 86% |
B6DZC8 | Triticum aestivum | 25% | 86% |
B6DZD0 | Triticum urartu | 26% | 86% |
B6DZD1 | Aegilops speltoides | 25% | 86% |
B6DZD2 | Aegilops tauschii | 26% | 86% |
D2IGW7 | Bromus pictus | 26% | 85% |
E1ABX2 | Aspergillus ficuum | 25% | 96% |
E8NHF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 98% |
E8NHF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
E9ACV4 | Leishmania major | 52% | 100% |
E9AK13 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 81% |
E9AWA3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AZE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
F8DVG5 | Zymomonas mobilis subsp. mobilis (strain ATCC 10988 / DSM 424 / LMG 404 / NCIMB 8938 / NRRL B-806 / ZM1) | 43% | 100% |
H2DF87 | Rosa hybrid cultivar | 29% | 87% |
H2DF88 | Rosa hybrid cultivar | 26% | 80% |
K0E681 | Aspergillus rugulosus | 27% | 100% |
O07003 | Bacillus subtilis (strain 168) | 26% | 99% |
O24509 | Phaseolus vulgaris | 26% | 79% |
O33833 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 33% | 100% |
O42878 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
O59852 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 88% |
O74641 | Aspergillus niger | 26% | 99% |
O74642 | Aspergillus niger | 26% | 99% |
O94220 | Aspergillus ficuum | 26% | 99% |
P00724 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 96% |
P05656 | Bacillus subtilis (strain 168) | 29% | 76% |
P07819 | Bacillus subtilis (strain 168) | 37% | 100% |
P0DJA7 | Zymomonas mobilis subsp. mobilis (strain ATCC 31821 / ZM4 / CP4) | 43% | 100% |
P10594 | Saccharomyces cerevisiae | 24% | 96% |
P10596 | Saccharomyces cerevisiae | 24% | 96% |
P13394 | Vibrio alginolyticus | 31% | 100% |
P13522 | Streptococcus mutans serotype c (strain ATCC 700610 / UA159) | 30% | 100% |
P16553 | Escherichia coli | 49% | 100% |
P24133 | Schwanniomyces occidentalis | 25% | 96% |
P26792 | Daucus carota | 24% | 87% |
P27217 | Klebsiella pneumoniae | 36% | 100% |
P28999 | Kluyveromyces marxianus | 24% | 92% |
P29000 | Solanum lycopersicum | 26% | 81% |
P29001 | Vigna radiata var. radiata | 25% | 79% |
P37075 | Salmonella typhimurium | 36% | 100% |
P40714 | Escherichia coli | 50% | 100% |
P40912 | Wickerhamomyces anomalus | 25% | 93% |
P43471 | Pediococcus pentosaceus | 27% | 100% |
P49174 | Zea mays | 27% | 87% |
P49175 | Zea mays | 26% | 77% |
P80065 | Daucus carota | 26% | 78% |
P92916 | Allium cepa | 24% | 84% |
P93761 | Capsicum annuum | 26% | 80% |
Q01IS7 | Oryza sativa subsp. indica | 26% | 86% |
Q01IS8 | Oryza sativa subsp. indica | 25% | 88% |
Q04937 | Lactococcus lactis subsp. lactis | 28% | 100% |
Q05936 | Staphylococcus xylosus | 30% | 100% |
Q0E0P0 | Oryza sativa subsp. japonica | 28% | 89% |
Q0J360 | Oryza sativa subsp. japonica | 24% | 86% |
Q0JDC5 | Oryza sativa subsp. japonica | 26% | 86% |
Q0JDC6 | Oryza sativa subsp. japonica | 25% | 88% |
Q1PEF8 | Arabidopsis thaliana | 25% | 87% |
Q2UXF7 | Triticum aestivum | 29% | 86% |
Q39041 | Arabidopsis thaliana | 24% | 77% |
Q39692 | Daucus carota | 29% | 87% |
Q39693 | Daucus carota | 29% | 88% |
Q43089 | Pisum sativum | 24% | 92% |
Q43348 | Arabidopsis thaliana | 26% | 79% |
Q43857 | Vicia faba | 24% | 80% |
Q43866 | Arabidopsis thaliana | 26% | 88% |
Q4QB76 | Leishmania major | 67% | 93% |
Q56660 | Vibrio cholerae | 33% | 94% |
Q56UD0 | Oryza sativa subsp. japonica | 26% | 86% |
Q56UD1 | Oryza sativa subsp. japonica | 23% | 95% |
Q5FC15 | Asparagus officinalis | 25% | 84% |
Q5JJV0 | Oryza sativa subsp. japonica | 27% | 87% |
Q67XZ3 | Arabidopsis thaliana | 27% | 86% |
Q70AT7 | Hordeum vulgare | 26% | 86% |
Q70XE6 | Beta vulgaris | 26% | 85% |
Q76HP6 | Aspergillus niger | 25% | 96% |
Q84LA1 | Triticum aestivum | 26% | 86% |
Q84PN8 | Triticum aestivum | 26% | 86% |
Q8W413 | Arabidopsis thaliana | 27% | 87% |
Q8W4S6 | Arabidopsis thaliana | 25% | 93% |
Q96TU3 | Aspergillus awamori | 24% | 96% |
Q9FSV7 | Festuca arundinacea | 24% | 78% |
Q9KLT6 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 32% | 94% |
Q9LIB9 | Arabidopsis thaliana | 23% | 90% |
Q9XTP3 | Leishmania major | 27% | 80% |