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. | yes | yes: 8 |
Pissara et al. | yes | yes: 36 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 21 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 22 |
GO:0110165 | cellular anatomical entity | 1 | 22 |
GO:0005654 | nucleoplasm | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 22 |
GO:0006807 | nitrogen compound metabolic process | 2 | 22 |
GO:0008152 | metabolic process | 1 | 22 |
GO:0019538 | protein metabolic process | 3 | 22 |
GO:0043170 | macromolecule metabolic process | 3 | 22 |
GO:0044238 | primary metabolic process | 2 | 22 |
GO:0071704 | organic substance metabolic process | 2 | 22 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 22 |
GO:0004177 | aminopeptidase activity | 5 | 22 |
GO:0005488 | binding | 1 | 22 |
GO:0008233 | peptidase activity | 3 | 22 |
GO:0008235 | metalloexopeptidase activity | 5 | 22 |
GO:0008237 | metallopeptidase activity | 4 | 22 |
GO:0008238 | exopeptidase activity | 4 | 22 |
GO:0016787 | hydrolase activity | 2 | 22 |
GO:0030145 | manganese ion binding | 6 | 22 |
GO:0043167 | ion binding | 2 | 22 |
GO:0043169 | cation binding | 3 | 22 |
GO:0046872 | metal ion binding | 4 | 22 |
GO:0046914 | transition metal ion binding | 5 | 22 |
GO:0070006 | metalloaminopeptidase activity | 6 | 22 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 22 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.284 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.550 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.435 |
CLV_Separin_Metazoa | 194 | 198 | PF03568 | 0.381 |
DEG_COP1_1 | 403 | 412 | PF00400 | 0.454 |
DEG_SPOP_SBC_1 | 105 | 109 | PF00917 | 0.260 |
DEG_SPOP_SBC_1 | 481 | 485 | PF00917 | 0.252 |
DOC_CKS1_1 | 220 | 225 | PF01111 | 0.492 |
DOC_CYCLIN_yCln2_LP_2 | 455 | 461 | PF00134 | 0.406 |
DOC_MAPK_gen_1 | 503 | 511 | PF00069 | 0.445 |
DOC_MAPK_gen_1 | 93 | 101 | PF00069 | 0.407 |
DOC_MAPK_MEF2A_6 | 176 | 185 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 503 | 511 | PF00069 | 0.415 |
DOC_MAPK_NFAT4_5 | 176 | 184 | PF00069 | 0.479 |
DOC_PP1_RVXF_1 | 60 | 67 | PF00149 | 0.284 |
DOC_PP4_FxxP_1 | 504 | 507 | PF00568 | 0.332 |
DOC_PP4_FxxP_1 | 66 | 69 | PF00568 | 0.355 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.380 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.381 |
DOC_USP7_UBL2_3 | 172 | 176 | PF12436 | 0.546 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.393 |
LIG_14-3-3_CanoR_1 | 188 | 196 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 197 | 202 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 343 | 352 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 93 | 101 | PF00244 | 0.516 |
LIG_Actin_WH2_2 | 46 | 64 | PF00022 | 0.252 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.613 |
LIG_BIR_III_4 | 388 | 392 | PF00653 | 0.365 |
LIG_BRCT_BRCA1_1 | 500 | 504 | PF00533 | 0.355 |
LIG_BRCT_BRCA1_1 | 62 | 66 | PF00533 | 0.391 |
LIG_DLG_GKlike_1 | 116 | 124 | PF00625 | 0.483 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.490 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.374 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.436 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.367 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.374 |
LIG_LIR_Apic_2 | 278 | 284 | PF02991 | 0.443 |
LIG_LIR_Apic_2 | 467 | 473 | PF02991 | 0.395 |
LIG_LIR_Apic_2 | 501 | 507 | PF02991 | 0.330 |
LIG_LIR_Apic_2 | 63 | 69 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 229 | 240 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 33 | 40 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 344 | 354 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 454 | 460 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 529 | 535 | PF02991 | 0.448 |
LIG_LYPXL_yS_3 | 457 | 460 | PF13949 | 0.332 |
LIG_Pex14_2 | 504 | 508 | PF04695 | 0.425 |
LIG_Pex14_3 | 530 | 535 | PF04695 | 0.314 |
LIG_SH2_CRK | 260 | 264 | PF00017 | 0.373 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.443 |
LIG_SH2_CRK | 470 | 474 | PF00017 | 0.362 |
LIG_SH2_NCK_1 | 232 | 236 | PF00017 | 0.492 |
LIG_SH2_SRC | 232 | 235 | PF00017 | 0.332 |
LIG_SH2_STAP1 | 163 | 167 | PF00017 | 0.550 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.393 |
LIG_SH2_STAP1 | 239 | 243 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 435 | 439 | PF00017 | 0.284 |
LIG_SH2_STAP1 | 96 | 100 | PF00017 | 0.395 |
LIG_SH2_STAT3 | 174 | 177 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.408 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.500 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.386 |
LIG_Sin3_3 | 332 | 339 | PF02671 | 0.492 |
LIG_SUMO_SIM_anti_2 | 371 | 378 | PF11976 | 0.409 |
LIG_SUMO_SIM_anti_2 | 381 | 388 | PF11976 | 0.409 |
LIG_TRAF2_1 | 130 | 133 | PF00917 | 0.394 |
LIG_TYR_ITIM | 230 | 235 | PF00017 | 0.492 |
LIG_TYR_ITIM | 455 | 460 | PF00017 | 0.332 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.530 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.397 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.530 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.474 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.449 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.516 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.453 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.365 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.465 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.541 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.516 |
MOD_Cter_Amidation | 91 | 94 | PF01082 | 0.284 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.709 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.452 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.486 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.381 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.397 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.380 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.485 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.430 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.511 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.453 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.394 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.483 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.517 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.422 |
MOD_N-GLC_1 | 350 | 355 | PF02516 | 0.470 |
MOD_N-GLC_1 | 481 | 486 | PF02516 | 0.302 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.373 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.478 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.314 |
MOD_NEK2_2 | 80 | 85 | PF00069 | 0.470 |
MOD_PIKK_1 | 189 | 195 | PF00454 | 0.547 |
MOD_PK_1 | 197 | 203 | PF00069 | 0.363 |
MOD_PK_1 | 8 | 14 | PF00069 | 0.571 |
MOD_PKB_1 | 6 | 14 | PF00069 | 0.532 |
MOD_Plk_1 | 13 | 19 | PF00069 | 0.513 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.355 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.433 |
MOD_Plk_1 | 350 | 356 | PF00069 | 0.498 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.464 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.486 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.284 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.409 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.431 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.571 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.443 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.393 |
TRG_DiLeu_BaEn_4 | 132 | 138 | PF01217 | 0.300 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 457 | 460 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.483 |
TRG_NES_CRM1_1 | 205 | 217 | PF08389 | 0.509 |
TRG_NLS_MonoCore_2 | 4 | 9 | PF00514 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 85 | 89 | PF00026 | 0.445 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8E6 | Leptomonas seymouri | 41% | 100% |
A0A0N1PAS4 | Leptomonas seymouri | 76% | 100% |
A0A0S4IQ79 | Bodo saltans | 41% | 100% |
A0A1X0NWR5 | Trypanosomatidae | 50% | 100% |
A0A1X0P4M9 | Trypanosomatidae | 40% | 100% |
A0A3R7JY84 | Trypanosoma rangeli | 50% | 100% |
A0A3R7N130 | Trypanosoma rangeli | 41% | 96% |
A0A3S7WRP1 | Leishmania donovani | 96% | 100% |
A0A3S7X742 | Leishmania donovani | 44% | 100% |
A4H6I8 | Leishmania braziliensis | 85% | 100% |
A4HLW7 | Leishmania braziliensis | 44% | 100% |
A4HUX3 | Leishmania infantum | 96% | 100% |
A4I996 | Leishmania infantum | 44% | 100% |
A6T0V4 | Janthinobacterium sp. (strain Marseille) | 30% | 100% |
A9IIK3 | Bordetella petrii (strain ATCC BAA-461 / DSM 12804 / CCUG 43448) | 30% | 100% |
B2JET5 | Paraburkholderia phymatum (strain DSM 17167 / CIP 108236 / LMG 21445 / STM815) | 28% | 100% |
B4F2N1 | Proteus mirabilis (strain HI4320) | 30% | 100% |
B8HTK3 | Cyanothece sp. (strain PCC 7425 / ATCC 29141) | 28% | 100% |
C4LA51 | Tolumonas auensis (strain DSM 9187 / TA4) | 30% | 100% |
C5CCM4 | Micrococcus luteus (strain ATCC 4698 / DSM 20030 / JCM 1464 / NBRC 3333 / NCIMB 9278 / NCTC 2665 / VKM Ac-2230) | 32% | 100% |
D0A654 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 95% |
D0A7H3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9ANK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9B496 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
P28838 | Homo sapiens | 28% | 100% |
P28839 | Sus scrofa | 27% | 100% |
Q1CTV6 | Helicobacter pylori (strain HPAG1) | 32% | 100% |
Q1H4U4 | Methylobacillus flagellatus (strain KT / ATCC 51484 / DSM 6875) | 28% | 100% |
Q1LJJ6 | Cupriavidus metallidurans (strain ATCC 43123 / DSM 2839 / NBRC 102507 / CH34) | 31% | 100% |
Q21KZ5 | Saccharophagus degradans (strain 2-40 / ATCC 43961 / DSM 17024) | 30% | 100% |
Q21WL3 | Albidiferax ferrireducens (strain ATCC BAA-621 / DSM 15236 / T118) | 30% | 100% |
Q2KWX0 | Bordetella avium (strain 197N) | 29% | 100% |
Q2YB18 | Nitrosospira multiformis (strain ATCC 25196 / NCIMB 11849 / C 71) | 29% | 100% |
Q315M7 | Oleidesulfovibrio alaskensis (strain ATCC BAA-1058 / DSM 17464 / G20) | 29% | 100% |
Q3M9J6 | Trichormus variabilis (strain ATCC 29413 / PCC 7937) | 28% | 100% |
Q46XT9 | Cupriavidus pinatubonensis (strain JMP 134 / LMG 1197) | 31% | 100% |
Q4Q3T0 | Leishmania major | 43% | 96% |
Q5FFZ5 | Ehrlichia ruminantium (strain Gardel) | 30% | 100% |
Q5HAP2 | Ehrlichia ruminantium (strain Welgevonden) | 30% | 100% |
Q5R7G6 | Pongo abelii | 37% | 100% |
Q68XM6 | Rickettsia typhi (strain ATCC VR-144 / Wilmington) | 29% | 100% |
Q6NSR8 | Mus musculus | 37% | 100% |
Q7W5K6 | Bordetella parapertussis (strain 12822 / ATCC BAA-587 / NCTC 13253) | 29% | 100% |
Q8D295 | Wigglesworthia glossinidia brevipalpis | 27% | 100% |
Q8KD74 | Chlorobaculum tepidum (strain ATCC 49652 / DSM 12025 / NBRC 103806 / TLS) | 33% | 100% |
Q8NDH3 | Homo sapiens | 37% | 100% |
Q9KTX5 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 32% | 100% |
Q9PH08 | Xylella fastidiosa (strain 9a5c) | 31% | 100% |
V5BTR1 | Trypanosoma cruzi | 41% | 97% |
V5BWE3 | Trypanosoma cruzi | 48% | 100% |