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: 95 |
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: 27, no: 5 |
NetGPI | no | yes: 0, no: 32 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0000323 | lytic vacuole | 6 | 3 |
GO:0005615 | extracellular space | 2 | 3 |
GO:0005764 | lysosome | 7 | 3 |
GO:0005773 | vacuole | 5 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
Related structures:
AlphaFold database: E8NHL3
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 33 |
GO:0006807 | nitrogen compound metabolic process | 2 | 33 |
GO:0008152 | metabolic process | 1 | 33 |
GO:0019538 | protein metabolic process | 3 | 33 |
GO:0043170 | macromolecule metabolic process | 3 | 33 |
GO:0044238 | primary metabolic process | 2 | 33 |
GO:0071704 | organic substance metabolic process | 2 | 33 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 33 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 33 |
GO:0004175 | endopeptidase activity | 4 | 24 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 24 |
GO:0008233 | peptidase activity | 3 | 33 |
GO:0008234 | cysteine-type peptidase activity | 4 | 33 |
GO:0016787 | hydrolase activity | 2 | 33 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 33 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 273 | 277 | PF00656 | 0.380 |
CLV_C14_Caspase3-7 | 512 | 516 | PF00656 | 0.486 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.469 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.394 |
CLV_PCSK_PC1ET2_1 | 132 | 134 | PF00082 | 0.639 |
CLV_PCSK_PC1ET2_1 | 199 | 201 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.411 |
CLV_Separin_Metazoa | 157 | 161 | PF03568 | 0.383 |
DEG_APCC_DBOX_1 | 209 | 217 | PF00400 | 0.455 |
DEG_APCC_DBOX_1 | 94 | 102 | PF00400 | 0.613 |
DEG_SPOP_SBC_1 | 436 | 440 | PF00917 | 0.399 |
DEG_SPOP_SBC_1 | 46 | 50 | PF00917 | 0.604 |
DOC_CDC14_PxL_1 | 17 | 25 | PF14671 | 0.583 |
DOC_CKS1_1 | 120 | 125 | PF01111 | 0.543 |
DOC_CKS1_1 | 511 | 516 | PF01111 | 0.310 |
DOC_CYCLIN_RxL_1 | 148 | 161 | PF00134 | 0.383 |
DOC_CYCLIN_yCln2_LP_2 | 8 | 14 | PF00134 | 0.565 |
DOC_MAPK_MEF2A_6 | 347 | 355 | PF00069 | 0.339 |
DOC_PP2B_LxvP_1 | 8 | 11 | PF13499 | 0.559 |
DOC_PP4_FxxP_1 | 511 | 514 | PF00568 | 0.258 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.278 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.655 |
DOC_USP7_UBL2_3 | 468 | 472 | PF12436 | 0.271 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.358 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.293 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.223 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.581 |
LIG_14-3-3_CanoR_1 | 40 | 46 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 467 | 471 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 57 | 63 | PF00244 | 0.581 |
LIG_BRCT_BRCA1_1 | 499 | 503 | PF00533 | 0.222 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.353 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.291 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.413 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.599 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.304 |
LIG_LIR_Gen_1 | 406 | 416 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 67 | 77 | PF02991 | 0.583 |
LIG_LIR_LC3C_4 | 319 | 324 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 390 | 396 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.589 |
LIG_LYPXL_yS_3 | 304 | 307 | PF13949 | 0.293 |
LIG_MYND_1 | 11 | 15 | PF01753 | 0.564 |
LIG_PCNA_PIPBox_1 | 170 | 179 | PF02747 | 0.250 |
LIG_PCNA_yPIPBox_3 | 165 | 177 | PF02747 | 0.250 |
LIG_SH2_GRB2like | 188 | 191 | PF00017 | 0.404 |
LIG_SH2_GRB2like | 499 | 502 | PF00017 | 0.374 |
LIG_SH2_PTP2 | 409 | 412 | PF00017 | 0.318 |
LIG_SH2_SRC | 188 | 191 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 499 | 503 | PF00017 | 0.222 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.595 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.507 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.580 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.567 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.660 |
LIG_Sin3_3 | 10 | 17 | PF02671 | 0.568 |
LIG_SUMO_SIM_par_1 | 259 | 265 | PF11976 | 0.331 |
LIG_SUMO_SIM_par_1 | 448 | 453 | PF11976 | 0.242 |
LIG_TRFH_1 | 80 | 84 | PF08558 | 0.582 |
LIG_TYR_ITIM | 391 | 396 | PF00017 | 0.380 |
MOD_CDC14_SPxK_1 | 490 | 493 | PF00782 | 0.222 |
MOD_CDK_SPK_2 | 22 | 27 | PF00069 | 0.581 |
MOD_CDK_SPK_2 | 70 | 75 | PF00069 | 0.581 |
MOD_CDK_SPxK_1 | 226 | 232 | PF00069 | 0.358 |
MOD_CDK_SPxK_1 | 487 | 493 | PF00069 | 0.222 |
MOD_CDK_SPxxK_3 | 441 | 448 | PF00069 | 0.314 |
MOD_CDK_SPxxK_3 | 510 | 517 | PF00069 | 0.324 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.384 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.328 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.330 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.579 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.371 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.320 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.311 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.297 |
MOD_GlcNHglycan | 212 | 216 | PF01048 | 0.718 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.615 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.528 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.593 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.548 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.503 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.390 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.483 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.341 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.664 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.350 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.638 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.388 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.575 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.587 |
MOD_N-GLC_1 | 460 | 465 | PF02516 | 0.472 |
MOD_N-GLC_2 | 417 | 419 | PF02516 | 0.540 |
MOD_N-GLC_2 | 474 | 476 | PF02516 | 0.536 |
MOD_N-GLC_2 | 528 | 530 | PF02516 | 0.521 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.421 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.432 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.286 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.385 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.729 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.382 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.741 |
MOD_PIKK_1 | 460 | 466 | PF00454 | 0.252 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.239 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.234 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.523 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.312 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.291 |
MOD_Plk_2-3 | 259 | 265 | PF00069 | 0.241 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.644 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.304 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.740 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.367 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.241 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.349 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.507 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.579 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.358 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.298 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.223 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.598 |
MOD_ProDKin_1 | 510 | 516 | PF00069 | 0.438 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.581 |
MOD_SUMO_rev_2 | 129 | 134 | PF00179 | 0.432 |
MOD_SUMO_rev_2 | 512 | 519 | PF00179 | 0.331 |
TRG_DiLeu_BaEn_4 | 144 | 150 | PF01217 | 0.365 |
TRG_DiLeu_BaLyEn_6 | 18 | 23 | PF01217 | 0.583 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.318 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.594 |
TRG_NES_CRM1_1 | 147 | 161 | PF08389 | 0.383 |
TRG_NLS_MonoExtC_3 | 206 | 212 | PF00514 | 0.490 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA65 | Leptomonas seymouri | 44% | 100% |
A0A0S4ISD8 | Bodo saltans | 41% | 100% |
A0A0S4J628 | Bodo saltans | 45% | 97% |
A0A0S4KJA5 | Bodo saltans | 42% | 100% |
A0A3R7L7E7 | Trypanosoma rangeli | 47% | 100% |
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 | 47% | 100% |
A5HII1 | Actinidia deliciosa | 31% | 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% |
E8NHJ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 100% | 100% |
E8NHS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 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) | 48% | 100% |
F4JNL3 | Arabidopsis thaliana | 31% | 100% |
P14658 | Trypanosoma brucei brucei | 46% | 100% |
P25779 | Trypanosoma cruzi | 47% | 100% |
P36400 | Leishmania mexicana | 100% | 100% |
P42666 | Plasmodium vivax (strain Salvador I) | 28% | 91% |
P43510 | Caenorhabditis elegans | 25% | 100% |
Q05094 | Leishmania pifanoi | 100% | 100% |
Q4QD68 | Leishmania major | 48% | 100% |
Q4QI61 | Leishmania major | 74% | 100% |
Q4QI66 | Leishmania major | 74% | 100% |
Q93VC9 | Arabidopsis thaliana | 27% | 100% |
Q9BIE1 | Leishmania donovani | 47% | 100% |