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: 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: Q4Q7T2
Term | Name | Level | Count |
---|---|---|---|
GO:0000045 | autophagosome assembly | 6 | 2 |
GO:0006508 | proteolysis | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0006810 | transport | 3 | 11 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007033 | vacuole organization | 5 | 2 |
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 | 2 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0033036 | macromolecule localization | 2 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 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:0070727 | cellular macromolecule localization | 3 | 11 |
GO:0070925 | organelle assembly | 5 | 2 |
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 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:1905037 | autophagosome organization | 6 | 2 |
GO:0006914 | autophagy | 3 | 9 |
GO:0009056 | catabolic process | 2 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044248 | cellular catabolic process | 3 | 9 |
GO:0061919 | process utilizing autophagic mechanism | 2 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 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_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.564 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.719 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.340 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.720 |
CLV_PCSK_PC1ET2_1 | 139 | 141 | PF00082 | 0.364 |
CLV_PCSK_PC1ET2_1 | 361 | 363 | PF00082 | 0.675 |
CLV_PCSK_PC7_1 | 357 | 363 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.489 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.639 |
DEG_SPOP_SBC_1 | 157 | 161 | PF00917 | 0.537 |
DOC_AGCK_PIF_1 | 45 | 50 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 94 | 100 | PF00069 | 0.564 |
DOC_MAPK_MEF2A_6 | 175 | 184 | PF00069 | 0.541 |
DOC_MAPK_MEF2A_6 | 272 | 281 | PF00069 | 0.541 |
DOC_PP1_RVXF_1 | 264 | 271 | PF00149 | 0.475 |
DOC_PP2B_LxvP_1 | 356 | 359 | PF13499 | 0.711 |
DOC_PP4_FxxP_1 | 327 | 330 | PF00568 | 0.708 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.547 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.701 |
LIG_14-3-3_CanoR_1 | 188 | 195 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 353 | 357 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 75 | 81 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 94 | 99 | PF00244 | 0.475 |
LIG_APCC_ABBA_1 | 96 | 101 | PF00400 | 0.564 |
LIG_APCC_ABBAyCdc20_2 | 95 | 101 | PF00400 | 0.564 |
LIG_BRCT_BRCA1_1 | 222 | 226 | PF00533 | 0.541 |
LIG_BRCT_BRCA1_1 | 296 | 300 | PF00533 | 0.562 |
LIG_BRCT_BRCA1_1 | 9 | 13 | PF00533 | 0.603 |
LIG_BRCT_BRCA1_1 | 96 | 100 | PF00533 | 0.514 |
LIG_Clathr_ClatBox_1 | 234 | 238 | PF01394 | 0.475 |
LIG_deltaCOP1_diTrp_1 | 7 | 13 | PF00928 | 0.606 |
LIG_EH1_1 | 108 | 116 | PF00400 | 0.513 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.532 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.519 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.465 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.725 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.702 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.459 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.533 |
LIG_FHA_2 | 282 | 288 | PF00498 | 0.494 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.607 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.530 |
LIG_LIR_Apic_2 | 127 | 131 | PF02991 | 0.479 |
LIG_LIR_Apic_2 | 324 | 330 | PF02991 | 0.709 |
LIG_LIR_Gen_1 | 198 | 207 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 275 | 283 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 287 | 296 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 297 | 304 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 387 | 394 | PF02991 | 0.719 |
LIG_LIR_Gen_1 | 42 | 50 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 52 | 60 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 7 | 17 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 198 | 203 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 223 | 227 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 275 | 281 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 287 | 292 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.720 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 7 | 12 | PF02991 | 0.578 |
LIG_MLH1_MIPbox_1 | 222 | 226 | PF16413 | 0.541 |
LIG_MLH1_MIPbox_1 | 9 | 13 | PF16413 | 0.603 |
LIG_MLH1_MIPbox_1 | 96 | 100 | PF16413 | 0.531 |
LIG_PCNA_PIPBox_1 | 78 | 87 | PF02747 | 0.541 |
LIG_PCNA_yPIPBox_3 | 75 | 85 | PF02747 | 0.513 |
LIG_Pex14_1 | 9 | 13 | PF04695 | 0.570 |
LIG_SH2_SRC | 236 | 239 | PF00017 | 0.485 |
LIG_SH2_STAP1 | 166 | 170 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.565 |
LIG_SUMO_SIM_anti_2 | 153 | 161 | PF11976 | 0.495 |
LIG_SUMO_SIM_anti_2 | 179 | 186 | PF11976 | 0.494 |
LIG_SUMO_SIM_par_1 | 179 | 186 | PF11976 | 0.497 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.530 |
LIG_TRFH_1 | 235 | 239 | PF08558 | 0.564 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.538 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.562 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.476 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.481 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.697 |
MOD_GlcNHglycan | 101 | 105 | PF01048 | 0.307 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.341 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.346 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.431 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.531 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.507 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.504 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.481 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.418 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.626 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.676 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.313 |
MOD_N-GLC_2 | 162 | 164 | PF02516 | 0.341 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.549 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.509 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.527 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.614 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.427 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.461 |
MOD_PIKK_1 | 129 | 135 | PF00454 | 0.475 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.492 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.505 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.596 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.475 |
MOD_PKA_1 | 94 | 100 | PF00069 | 0.531 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.521 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.717 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.475 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.513 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.450 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.632 |
MOD_Plk_2-3 | 386 | 392 | PF00069 | 0.723 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.551 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.474 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.678 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.426 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.526 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.468 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.515 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.701 |
MOD_SUMO_for_1 | 124 | 127 | PF00179 | 0.541 |
MOD_SUMO_for_1 | 146 | 149 | PF00179 | 0.564 |
TRG_DiLeu_BaLyEn_6 | 59 | 64 | PF01217 | 0.541 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.461 |
TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.750 |
TRG_NLS_MonoExtC_3 | 359 | 364 | PF00514 | 0.673 |
TRG_NLS_MonoExtN_4 | 357 | 364 | PF00514 | 0.673 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A098DRK7 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 26% | 84% |
A0A0N0P8C0 | Leptomonas seymouri | 64% | 98% |
A0A0S4JSC7 | Bodo saltans | 36% | 100% |
A0A1X0P2H1 | Trypanosomatidae | 39% | 100% |
A0A3R7NRV7 | Trypanosoma rangeli | 42% | 100% |
A0A3S7X2Y6 | Leishmania donovani | 94% | 100% |
A0A422NI42 | Trypanosoma rangeli | 27% | 100% |
A1CJ08 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 26% | 98% |
A2Q1V6 | Medicago truncatula | 25% | 81% |
A2QY50 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 27% | 98% |
A4HHX1 | Leishmania braziliensis | 84% | 99% |
A4I521 | Leishmania infantum | 94% | 100% |
A6SDQ3 | Botryotinia fuckeliana (strain B05.10) | 27% | 90% |
A7KAI3 | Pichia angusta | 30% | 77% |
A7KAL5 | Penicillium rubens (strain ATCC 28089 / DSM 1075 / NRRL 1951 / Wisconsin 54-1255) | 27% | 98% |
D0AAK8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
E9B0F1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
K8ESC5 | Caenorhabditis elegans | 25% | 82% |
Q0U199 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 26% | 84% |
Q1E5M9 | Coccidioides immitis (strain RS) | 27% | 91% |
Q2HH40 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 25% | 88% |
Q2U5B0 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 28% | 97% |
Q523C3 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 28% | 80% |
Q5B7L0 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 25% | 98% |
Q68FJ9 | Xenopus laevis | 22% | 84% |
Q6CH28 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 24% | 72% |
Q6FP20 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 21% | 82% |
Q86ZL5 | Podospora anserina | 24% | 79% |
Q8BGE6 | Mus musculus | 25% | 100% |
Q9P373 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
Q9Y4P1 | Homo sapiens | 25% | 100% |
V5AXZ8 | Trypanosoma cruzi | 25% | 100% |
V5BGZ3 | Trypanosoma cruzi | 40% | 100% |