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: 125 |
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: 21 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 33, no: 5 |
NetGPI | no | yes: 0, no: 38 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0000323 | lytic vacuole | 6 | 8 |
GO:0005615 | extracellular space | 2 | 8 |
GO:0005764 | lysosome | 7 | 8 |
GO:0005773 | vacuole | 5 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0043229 | intracellular organelle | 3 | 8 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 8 |
Related structures:
AlphaFold database: E8NHJ1
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 39 |
GO:0006807 | nitrogen compound metabolic process | 2 | 39 |
GO:0008152 | metabolic process | 1 | 39 |
GO:0019538 | protein metabolic process | 3 | 39 |
GO:0043170 | macromolecule metabolic process | 3 | 39 |
GO:0044238 | primary metabolic process | 2 | 39 |
GO:0071704 | organic substance metabolic process | 2 | 39 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 39 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 39 |
GO:0004175 | endopeptidase activity | 4 | 29 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 29 |
GO:0008233 | peptidase activity | 3 | 39 |
GO:0008234 | cysteine-type peptidase activity | 4 | 39 |
GO:0016787 | hydrolase activity | 2 | 39 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 39 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 243 | 247 | PF00656 | 0.389 |
CLV_C14_Caspase3-7 | 482 | 486 | PF00656 | 0.492 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.477 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.390 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 169 | 171 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.407 |
CLV_Separin_Metazoa | 127 | 131 | PF03568 | 0.386 |
DEG_APCC_DBOX_1 | 179 | 187 | PF00400 | 0.472 |
DEG_APCC_DBOX_1 | 64 | 72 | PF00400 | 0.612 |
DEG_SPOP_SBC_1 | 16 | 20 | PF00917 | 0.600 |
DEG_SPOP_SBC_1 | 406 | 410 | PF00917 | 0.301 |
DOC_CKS1_1 | 481 | 486 | PF01111 | 0.309 |
DOC_CKS1_1 | 90 | 95 | PF01111 | 0.541 |
DOC_CYCLIN_RxL_1 | 118 | 131 | PF00134 | 0.386 |
DOC_MAPK_MEF2A_6 | 317 | 325 | PF00069 | 0.413 |
DOC_PP4_FxxP_1 | 481 | 484 | PF00568 | 0.261 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.317 |
DOC_USP7_UBL2_3 | 438 | 442 | PF12436 | 0.276 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.223 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.518 |
LIG_14-3-3_CanoR_1 | 10 | 16 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 27 | 33 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 437 | 441 | PF00244 | 0.371 |
LIG_BRCT_BRCA1_1 | 469 | 473 | PF00533 | 0.222 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.347 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.447 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.586 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.393 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.308 |
LIG_LIR_Gen_1 | 37 | 47 | PF02991 | 0.772 |
LIG_LIR_Gen_1 | 376 | 386 | PF02991 | 0.365 |
LIG_LIR_LC3C_4 | 289 | 294 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 144 | 149 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 360 | 366 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.777 |
LIG_LIR_Nem_3 | 376 | 382 | PF02991 | 0.304 |
LIG_LYPXL_yS_3 | 274 | 277 | PF13949 | 0.296 |
LIG_PCNA_PIPBox_1 | 140 | 149 | PF02747 | 0.244 |
LIG_PCNA_yPIPBox_3 | 135 | 147 | PF02747 | 0.244 |
LIG_SH2_GRB2like | 158 | 161 | PF00017 | 0.407 |
LIG_SH2_GRB2like | 469 | 472 | PF00017 | 0.379 |
LIG_SH2_PTP2 | 379 | 382 | PF00017 | 0.321 |
LIG_SH2_SRC | 158 | 161 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.341 |
LIG_SH2_STAP1 | 469 | 473 | PF00017 | 0.222 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.403 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.663 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.503 |
LIG_SUMO_SIM_par_1 | 229 | 235 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 418 | 423 | PF11976 | 0.241 |
LIG_TRFH_1 | 50 | 54 | PF08558 | 0.578 |
LIG_TYR_ITIM | 361 | 366 | PF00017 | 0.391 |
MOD_CDC14_SPxK_1 | 460 | 463 | PF00782 | 0.222 |
MOD_CDK_SPK_2 | 40 | 45 | PF00069 | 0.583 |
MOD_CDK_SPxK_1 | 196 | 202 | PF00069 | 0.368 |
MOD_CDK_SPxK_1 | 457 | 463 | PF00069 | 0.222 |
MOD_CDK_SPxxK_3 | 411 | 418 | PF00069 | 0.316 |
MOD_CDK_SPxxK_3 | 480 | 487 | PF00069 | 0.323 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.370 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.329 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.317 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.578 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.375 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.321 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.309 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.295 |
MOD_GlcNHglycan | 182 | 186 | PF01048 | 0.727 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.620 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.529 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.589 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.389 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.555 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.509 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.463 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.765 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.659 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.340 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.359 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.393 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.574 |
MOD_N-GLC_1 | 287 | 292 | PF02516 | 0.598 |
MOD_N-GLC_1 | 430 | 435 | PF02516 | 0.478 |
MOD_N-GLC_2 | 387 | 389 | PF02516 | 0.540 |
MOD_N-GLC_2 | 444 | 446 | PF02516 | 0.542 |
MOD_N-GLC_2 | 498 | 500 | PF02516 | 0.529 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.427 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.419 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.722 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.298 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.392 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.391 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.749 |
MOD_PIKK_1 | 430 | 436 | PF00454 | 0.257 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.238 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.234 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.531 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.315 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.296 |
MOD_Plk_2-3 | 229 | 235 | PF00069 | 0.244 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.592 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.309 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.376 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.245 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.355 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.597 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.368 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.582 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.308 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.223 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.442 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.513 |
MOD_SUMO_rev_2 | 482 | 489 | PF00179 | 0.329 |
MOD_SUMO_rev_2 | 99 | 104 | PF00179 | 0.434 |
TRG_DiLeu_BaEn_4 | 114 | 120 | PF01217 | 0.373 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 363 | 366 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.321 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.590 |
TRG_NES_CRM1_1 | 117 | 131 | PF08389 | 0.386 |
TRG_NLS_MonoExtC_3 | 176 | 182 | PF00514 | 0.495 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8D1 | Leptomonas seymouri | 26% | 100% |
A0A0N1PA65 | Leptomonas seymouri | 44% | 100% |
A0A0S4ISD8 | Bodo saltans | 41% | 94% |
A0A0S4J628 | Bodo saltans | 45% | 92% |
A0A0S4JXJ3 | Bodo saltans | 31% | 100% |
A0A0S4KJA5 | Bodo saltans | 42% | 100% |
A0A1X0NXC8 | Trypanosomatidae | 32% | 100% |
A0A3R7L7E7 | Trypanosoma rangeli | 47% | 95% |
A0A3S5H682 | Leishmania donovani | 80% | 100% |
A0A3S5H683 | Leishmania donovani | 80% | 100% |
A0A3S5H684 | Leishmania donovani | 80% | 100% |
A0A3S5H685 | Leishmania donovani | 80% | 100% |
A0A3S7WQD0 | Leishmania donovani | 80% | 100% |
A0A6L0WJ22 | Leishmania infantum | 81% | 100% |
A4H5E4 | Leishmania braziliensis | 67% | 100% |
A4H5E5 | Leishmania braziliensis | 65% | 100% |
A4H5E6 | Leishmania braziliensis | 65% | 100% |
A4HA92 | Leishmania braziliensis | 44% | 100% |
A4HTP0 | Leishmania infantum | 78% | 100% |
A4HYH2 | Leishmania infantum | 45% | 100% |
A4I4D6 | Leishmania infantum | 32% | 100% |
A5HII1 | Actinidia deliciosa | 30% | 100% |
C9ZQB3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
C9ZQB5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
C9ZQB6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E8NHD8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
E8NHH6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
E8NHL3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 100% | 94% |
E8NHS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
E9ADT5 | Leishmania major | 30% | 100% |
E9ALZ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AMH5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
E9AMH6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
E9AMH7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
E9AS96 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
F4JNL3 | Arabidopsis thaliana | 31% | 100% |
O65493 | Arabidopsis thaliana | 36% | 100% |
P00785 | Actinidia chinensis var. chinensis | 31% | 100% |
P04988 | Dictyostelium discoideum | 36% | 100% |
P14658 | Trypanosoma brucei brucei | 46% | 100% |
P25775 | Leishmania mexicana | 46% | 100% |
P25779 | Trypanosoma cruzi | 47% | 100% |
P25805 | Plasmodium falciparum | 28% | 88% |
P35591 | Leishmania pifanoi | 46% | 100% |
P36400 | Leishmania mexicana | 100% | 100% |
P42666 | Plasmodium vivax (strain Salvador I) | 28% | 86% |
P43156 | Hemerocallis sp. | 37% | 100% |
P46102 | Plasmodium vinckei | 30% | 99% |
P54640 | Dictyostelium discoideum | 34% | 100% |
P56202 | Homo sapiens | 32% | 100% |
Q05094 | Leishmania pifanoi | 100% | 100% |
Q23894 | Dictyostelium discoideum | 34% | 100% |
Q4QD68 | Leishmania major | 48% | 100% |
Q4QI61 | Leishmania major | 74% | 100% |
Q4QI62 | Leishmania major | 85% | 100% |
Q4QI64 | Leishmania major | 85% | 100% |
Q4QI65 | Leishmania major | 85% | 100% |
Q4QI66 | Leishmania major | 74% | 100% |
Q4QI67 | Leishmania major | 85% | 100% |
Q4QI68 | Leishmania major | 84% | 100% |
Q7GDU7 | Oryza sativa subsp. japonica | 36% | 100% |
Q8QLK1 | Mamestra configurata nucleopolyhedrovirus | 35% | 100% |
Q9BIE1 | Leishmania donovani | 45% | 100% |
Q9GQM5 | Leishmania donovani | 32% | 100% |
Q9LT78 | Arabidopsis thaliana | 36% | 100% |
Q9QZE3 | Rattus norvegicus | 33% | 100% |
Q9SUT0 | Arabidopsis thaliana | 34% | 100% |