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. | yes | yes: 5 |
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: 4 |
NetGPI | no | yes: 0, no: 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4H334
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0019538 | protein metabolic process | 3 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 5 |
GO:0004175 | endopeptidase activity | 4 | 5 |
GO:0004190 | aspartic-type endopeptidase activity | 5 | 5 |
GO:0008233 | peptidase activity | 3 | 5 |
GO:0016787 | hydrolase activity | 2 | 5 |
GO:0070001 | aspartic-type peptidase activity | 4 | 5 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.209 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.761 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.209 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.213 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.772 |
CLV_PCSK_PC1ET2_1 | 216 | 218 | PF00082 | 0.209 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.732 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.383 |
DEG_SCF_TRCP1_1 | 206 | 212 | PF00400 | 0.393 |
DEG_SIAH_1 | 139 | 147 | PF03145 | 0.504 |
DEG_SPOP_SBC_1 | 95 | 99 | PF00917 | 0.456 |
DOC_CDC14_PxL_1 | 370 | 378 | PF14671 | 0.456 |
DOC_MAPK_gen_1 | 231 | 239 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 282 | 290 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 381 | 391 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 231 | 239 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 282 | 290 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 85 | 93 | PF00069 | 0.350 |
DOC_PP1_RVXF_1 | 299 | 305 | PF00149 | 0.308 |
DOC_PP2B_LxvP_1 | 190 | 193 | PF13499 | 0.453 |
DOC_PP2B_LxvP_1 | 92 | 95 | PF13499 | 0.391 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.790 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.591 |
DOC_USP7_UBL2_3 | 198 | 202 | PF12436 | 0.413 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.453 |
LIG_14-3-3_CanoR_1 | 10 | 15 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 16 | 20 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 186 | 190 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 50 | 58 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 96 | 106 | PF00244 | 0.488 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.526 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.397 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.420 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.414 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.466 |
LIG_LIR_Gen_1 | 182 | 192 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 292 | 302 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 387 | 394 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 408 | 417 | PF02991 | 0.237 |
LIG_LIR_LC3C_4 | 87 | 91 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 182 | 187 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 292 | 297 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 387 | 391 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 408 | 412 | PF02991 | 0.237 |
LIG_PCNA_yPIPBox_3 | 216 | 228 | PF02747 | 0.409 |
LIG_PROFILIN_1 | 125 | 131 | PF00235 | 0.536 |
LIG_Rb_pABgroove_1 | 111 | 119 | PF01858 | 0.519 |
LIG_SH2_CRK | 161 | 165 | PF00017 | 0.354 |
LIG_SH2_NCK_1 | 161 | 165 | PF00017 | 0.359 |
LIG_SH2_SRC | 294 | 297 | PF00017 | 0.245 |
LIG_SH2_STAP1 | 315 | 319 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.425 |
LIG_SH3_1 | 308 | 314 | PF00018 | 0.387 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.543 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.625 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.330 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.433 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.546 |
LIG_SUMO_SIM_anti_2 | 68 | 76 | PF11976 | 0.349 |
LIG_SUMO_SIM_anti_2 | 87 | 94 | PF11976 | 0.273 |
LIG_SUMO_SIM_par_1 | 286 | 292 | PF11976 | 0.398 |
LIG_UBA3_1 | 286 | 291 | PF00899 | 0.490 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.619 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.372 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.499 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.639 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.445 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.570 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.233 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.483 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.405 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.530 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.566 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.367 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.678 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.661 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.389 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.485 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.553 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.665 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.728 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.489 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.659 |
MOD_N-GLC_1 | 6 | 11 | PF02516 | 0.334 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.547 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.408 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.215 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.527 |
MOD_NEK2_2 | 355 | 360 | PF00069 | 0.525 |
MOD_PIKK_1 | 120 | 126 | PF00454 | 0.549 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.658 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.368 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.409 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.590 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.409 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.482 |
MOD_Plk_2-3 | 268 | 274 | PF00069 | 0.409 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.490 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.413 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.294 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.337 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.537 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.304 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.453 |
MOD_SUMO_for_1 | 84 | 87 | PF00179 | 0.330 |
MOD_SUMO_rev_2 | 392 | 400 | PF00179 | 0.237 |
TRG_DiLeu_BaEn_1 | 220 | 225 | PF01217 | 0.413 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.425 |
TRG_ER_diArg_1 | 230 | 233 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.775 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJX8 | Leptomonas seymouri | 40% | 91% |
A0A1X0P3Q1 | Trypanosomatidae | 44% | 100% |
I7HUG0 | Leishmania major | 62% | 100% |
P0CS14 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 37% | 97% |
P0CS15 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 37% | 97% |
Q1DNB9 | Coccidioides immitis (strain RS) | 39% | 94% |
V5BLJ9 | Trypanosoma cruzi | 40% | 88% |