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: 3 |
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: Q4Q4N3
Term | Name | Level | Count |
---|---|---|---|
GO:0000045 | autophagosome assembly | 6 | 11 |
GO:0006508 | proteolysis | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0006810 | transport | 3 | 11 |
GO:0006996 | organelle organization | 4 | 11 |
GO:0007033 | vacuole organization | 5 | 11 |
GO:0008104 | protein localization | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0015031 | protein transport | 4 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0022607 | cellular component assembly | 4 | 11 |
GO:0033036 | macromolecule localization | 2 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0045184 | establishment of protein localization | 3 | 11 |
GO:0051179 | localization | 1 | 11 |
GO:0051234 | establishment of localization | 2 | 11 |
GO:0051641 | cellular localization | 2 | 11 |
GO:0051697 | protein delipidation | 5 | 11 |
GO:0070727 | cellular macromolecule localization | 3 | 11 |
GO:0070925 | organelle assembly | 5 | 11 |
GO:0071702 | organic substance transport | 4 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0071705 | nitrogen compound transport | 4 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:1905037 | autophagosome organization | 6 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004175 | endopeptidase activity | 4 | 11 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 11 |
GO:0008233 | peptidase activity | 3 | 11 |
GO:0008234 | cysteine-type peptidase activity | 4 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.233 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.366 |
CLV_PCSK_FUR_1 | 289 | 293 | PF00082 | 0.142 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.208 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.214 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.255 |
DEG_ODPH_VHL_1 | 218 | 230 | PF01847 | 0.377 |
DEG_SPOP_SBC_1 | 271 | 275 | PF00917 | 0.384 |
DOC_CKS1_1 | 30 | 35 | PF01111 | 0.362 |
DOC_CKS1_1 | 303 | 308 | PF01111 | 0.400 |
DOC_CYCLIN_RxL_1 | 61 | 71 | PF00134 | 0.246 |
DOC_CYCLIN_yCln2_LP_2 | 210 | 216 | PF00134 | 0.369 |
DOC_MAPK_gen_1 | 126 | 134 | PF00069 | 0.499 |
DOC_MAPK_gen_1 | 289 | 299 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 35 | 45 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 292 | 301 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 38 | 46 | PF00069 | 0.285 |
DOC_PP1_RVXF_1 | 256 | 263 | PF00149 | 0.452 |
DOC_PP1_RVXF_1 | 64 | 71 | PF00149 | 0.470 |
DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.369 |
DOC_PP4_FxxP_1 | 262 | 265 | PF00568 | 0.389 |
DOC_PP4_FxxP_1 | 30 | 33 | PF00568 | 0.363 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.454 |
DOC_USP7_UBL2_3 | 150 | 154 | PF12436 | 0.377 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.464 |
DOC_USP7_UBL2_3 | 61 | 65 | PF12436 | 0.235 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.370 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.431 |
LIG_14-3-3_CanoR_1 | 344 | 349 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 94 | 100 | PF00244 | 0.377 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.409 |
LIG_BRCT_BRCA1_1 | 258 | 262 | PF00533 | 0.374 |
LIG_BRCT_BRCA1_1 | 26 | 30 | PF00533 | 0.348 |
LIG_EVH1_1 | 76 | 80 | PF00568 | 0.377 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.363 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.246 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.196 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.408 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.452 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.418 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.667 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.461 |
LIG_LIR_Apic_2 | 259 | 265 | PF02991 | 0.372 |
LIG_LIR_Apic_2 | 27 | 33 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 128 | 139 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 152 | 161 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 222 | 233 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 56 | 67 | PF02991 | 0.288 |
LIG_LIR_LC3C_4 | 321 | 324 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 307 | 312 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.531 |
LIG_MLH1_MIPbox_1 | 258 | 262 | PF16413 | 0.390 |
LIG_PTAP_UEV_1 | 134 | 139 | PF05743 | 0.369 |
LIG_SH2_PTP2 | 113 | 116 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 155 | 159 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 225 | 229 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.377 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.369 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.351 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.452 |
LIG_SUMO_SIM_anti_2 | 40 | 48 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 341 | 351 | PF11976 | 0.617 |
LIG_SUMO_SIM_par_1 | 40 | 48 | PF11976 | 0.397 |
LIG_UBA3_1 | 229 | 236 | PF00899 | 0.375 |
LIG_WRC_WIRS_1 | 327 | 332 | PF05994 | 0.523 |
LIG_WW_2 | 77 | 80 | PF00397 | 0.377 |
MOD_CDK_SPxK_1 | 29 | 35 | PF00069 | 0.362 |
MOD_CDK_SPxxK_3 | 29 | 36 | PF00069 | 0.364 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.407 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.391 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.516 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.643 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.548 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.523 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.380 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.600 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.693 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.546 |
MOD_Cter_Amidation | 330 | 333 | PF01082 | 0.275 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.170 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.239 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.542 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.281 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.311 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.142 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.378 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.761 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.732 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.366 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.413 |
MOD_N-GLC_1 | 38 | 43 | PF02516 | 0.450 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.467 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.443 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.369 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.381 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.452 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.452 |
MOD_PK_1 | 344 | 350 | PF00069 | 0.444 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.365 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.492 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.452 |
MOD_PKB_1 | 333 | 341 | PF00069 | 0.422 |
MOD_Plk_2-3 | 336 | 342 | PF00069 | 0.422 |
MOD_Plk_2-3 | 353 | 359 | PF00069 | 0.460 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.341 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.403 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.427 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.334 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.380 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.481 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.370 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.395 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.470 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 323 | 328 | PF01217 | 0.271 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.377 |
TRG_ER_diArg_1 | 288 | 291 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 332 | 335 | PF00400 | 0.345 |
TRG_NES_CRM1_1 | 122 | 133 | PF08389 | 0.455 |
TRG_NLS_MonoExtN_4 | 33 | 39 | PF00514 | 0.329 |
TRG_Pf-PMV_PEXEL_1 | 191 | 195 | PF00026 | 0.177 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A098DRK7 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 22% | 83% |
A0A0N0P8C0 | Leptomonas seymouri | 28% | 97% |
A0A0N1IIY5 | Leptomonas seymouri | 60% | 100% |
A0A0S4JSC7 | Bodo saltans | 26% | 100% |
A0A1X0NS04 | Trypanosomatidae | 35% | 100% |
A0A1X0P2H1 | Trypanosomatidae | 25% | 100% |
A0A3S7X6B3 | Leishmania donovani | 89% | 100% |
A0A422NI42 | Trypanosoma rangeli | 37% | 100% |
A1CJ08 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 25% | 97% |
A2QY50 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 26% | 96% |
A4HL26 | Leishmania braziliensis | 76% | 97% |
A4I8K7 | Leishmania infantum | 88% | 100% |
A5DEF7 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 30% | 97% |
A5DSB4 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 24% | 74% |
A6ZRL7 | Saccharomyces cerevisiae (strain YJM789) | 27% | 79% |
A7KAL5 | Penicillium rubens (strain ATCC 28089 / DSM 1075 / NRRL 1951 / Wisconsin 54-1255) | 25% | 97% |
A7TQN1 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 27% | 94% |
D0AAK8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E2RDP2 | Canis lupus familiaris | 24% | 82% |
E9B3G7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
P53867 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 79% |
Q1E5M9 | Coccidioides immitis (strain RS) | 26% | 90% |
Q2HH40 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 24% | 87% |
Q2U5B0 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 27% | 95% |
Q4U3V5 | Cryphonectria parasitica | 26% | 85% |
Q523C3 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 26% | 79% |
Q59UG3 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 24% | 87% |
Q5B7L0 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 22% | 97% |
Q5XH30 | Xenopus laevis | 26% | 86% |
Q684M2 | Sus scrofa | 25% | 83% |
Q68EP9 | Xenopus tropicalis | 24% | 86% |
Q68FJ9 | Xenopus laevis | 24% | 83% |
Q6CH28 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 26% | 71% |
Q6FP20 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 25% | 80% |
Q6PZ02 | Gallus gallus | 21% | 99% |
Q75KP8 | Oryza sativa subsp. japonica | 23% | 82% |
Q811C2 | Mus musculus | 25% | 85% |
Q86TL0 | Homo sapiens | 25% | 82% |
Q8BGV9 | Mus musculus | 24% | 82% |
Q8S929 | Arabidopsis thaliana | 24% | 83% |
Q96DT6 | Homo sapiens | 25% | 85% |
Q9M1Y0 | Arabidopsis thaliana | 23% | 81% |
Q9P373 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
V5AXZ8 | Trypanosoma cruzi | 37% | 100% |