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: 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. | no | 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: 20 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 21 |
GO:0110165 | cellular anatomical entity | 1 | 21 |
GO:0005654 | nucleoplasm | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 21 |
GO:0006807 | nitrogen compound metabolic process | 2 | 21 |
GO:0008152 | metabolic process | 1 | 21 |
GO:0019538 | protein metabolic process | 3 | 21 |
GO:0043170 | macromolecule metabolic process | 3 | 21 |
GO:0044238 | primary metabolic process | 2 | 21 |
GO:0071704 | organic substance metabolic process | 2 | 21 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 21 |
GO:0004177 | aminopeptidase activity | 5 | 21 |
GO:0005488 | binding | 1 | 21 |
GO:0008233 | peptidase activity | 3 | 21 |
GO:0008235 | metalloexopeptidase activity | 5 | 21 |
GO:0008237 | metallopeptidase activity | 4 | 21 |
GO:0008238 | exopeptidase activity | 4 | 21 |
GO:0016787 | hydrolase activity | 2 | 21 |
GO:0030145 | manganese ion binding | 6 | 21 |
GO:0043167 | ion binding | 2 | 21 |
GO:0043169 | cation binding | 3 | 21 |
GO:0046872 | metal ion binding | 4 | 21 |
GO:0046914 | transition metal ion binding | 5 | 21 |
GO:0070006 | metalloaminopeptidase activity | 6 | 21 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 21 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.516 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.324 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.418 |
DEG_SPOP_SBC_1 | 4 | 8 | PF00917 | 0.405 |
DOC_CKS1_1 | 217 | 222 | PF01111 | 0.442 |
DOC_CYCLIN_yCln2_LP_2 | 452 | 458 | PF00134 | 0.392 |
DOC_MAPK_gen_1 | 192 | 200 | PF00069 | 0.331 |
DOC_MAPK_gen_1 | 500 | 508 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 173 | 182 | PF00069 | 0.371 |
DOC_MAPK_MEF2A_6 | 500 | 508 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 90 | 98 | PF00069 | 0.412 |
DOC_MAPK_NFAT4_5 | 173 | 181 | PF00069 | 0.435 |
DOC_PP4_FxxP_1 | 501 | 504 | PF00568 | 0.356 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.273 |
DOC_USP7_UBL2_3 | 165 | 169 | PF12436 | 0.504 |
DOC_USP7_UBL2_3 | 192 | 196 | PF12436 | 0.294 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.384 |
LIG_14-3-3_CanoR_1 | 185 | 193 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 194 | 199 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 3 | 10 | PF00244 | 0.493 |
LIG_BIR_III_4 | 385 | 389 | PF00653 | 0.342 |
LIG_BRCT_BRCA1_1 | 27 | 31 | PF00533 | 0.270 |
LIG_BRCT_BRCA1_1 | 497 | 501 | PF00533 | 0.354 |
LIG_BRCT_BRCA1_1 | 59 | 63 | PF00533 | 0.339 |
LIG_CtBP_PxDLS_1 | 249 | 255 | PF00389 | 0.369 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.448 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.378 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.323 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.325 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.342 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.489 |
LIG_HP1_1 | 42 | 46 | PF01393 | 0.190 |
LIG_LIR_Apic_2 | 275 | 281 | PF02991 | 0.467 |
LIG_LIR_Apic_2 | 464 | 470 | PF02991 | 0.377 |
LIG_LIR_Apic_2 | 498 | 504 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 135 | 144 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 226 | 237 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 28 | 37 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 341 | 351 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 135 | 140 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 226 | 232 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 28 | 34 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 341 | 346 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.342 |
LIG_LYPXL_yS_3 | 454 | 457 | PF13949 | 0.356 |
LIG_Pex14_2 | 501 | 505 | PF04695 | 0.426 |
LIG_Pex14_3 | 527 | 532 | PF04695 | 0.296 |
LIG_SH2_CRK | 257 | 261 | PF00017 | 0.351 |
LIG_SH2_CRK | 278 | 282 | PF00017 | 0.467 |
LIG_SH2_CRK | 467 | 471 | PF00017 | 0.388 |
LIG_SH2_NCK_1 | 229 | 233 | PF00017 | 0.442 |
LIG_SH2_PTP2 | 137 | 140 | PF00017 | 0.190 |
LIG_SH2_SRC | 229 | 232 | PF00017 | 0.290 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.341 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.284 |
LIG_SH2_STAT3 | 171 | 174 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.357 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.433 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.322 |
LIG_Sin3_3 | 329 | 336 | PF02671 | 0.467 |
LIG_SUMO_SIM_anti_2 | 368 | 375 | PF11976 | 0.395 |
LIG_SUMO_SIM_anti_2 | 378 | 385 | PF11976 | 0.395 |
LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.342 |
LIG_TRAF2_1 | 9 | 12 | PF00917 | 0.504 |
LIG_TYR_ITIM | 227 | 232 | PF00017 | 0.442 |
LIG_TYR_ITIM | 452 | 457 | PF00017 | 0.356 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.416 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.440 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.474 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.351 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.441 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.392 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.466 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.401 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.342 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.462 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.475 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.441 |
MOD_GlcNHglycan | 11 | 15 | PF01048 | 0.432 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.368 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.451 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.351 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.353 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.463 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.255 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.507 |
MOD_GlcNHglycan | 86 | 90 | PF01048 | 0.304 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.417 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.284 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.387 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.396 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.407 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.198 |
MOD_N-GLC_1 | 347 | 352 | PF02516 | 0.449 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.331 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.338 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.458 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.464 |
MOD_NEK2_2 | 77 | 82 | PF00069 | 0.420 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.508 |
MOD_PK_1 | 113 | 119 | PF00069 | 0.402 |
MOD_PK_1 | 194 | 200 | PF00069 | 0.327 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.365 |
MOD_PKB_1 | 3 | 11 | PF00069 | 0.483 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.457 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.516 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.198 |
MOD_Plk_1 | 347 | 353 | PF00069 | 0.461 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.402 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.420 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.436 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.392 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.395 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.384 |
MOD_SUMO_for_1 | 172 | 175 | PF00179 | 0.266 |
MOD_SUMO_for_1 | 247 | 250 | PF00179 | 0.431 |
TRG_DiLeu_BaEn_4 | 129 | 135 | PF01217 | 0.256 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.190 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.366 |
TRG_NES_CRM1_1 | 202 | 214 | PF08389 | 0.460 |
TRG_NLS_MonoCore_2 | 1 | 6 | PF00514 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 82 | 86 | PF00026 | 0.382 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8E6 | Leptomonas seymouri | 43% | 100% |
A0A0N1PAS4 | Leptomonas seymouri | 76% | 99% |
A0A0S4IQ79 | Bodo saltans | 42% | 100% |
A0A1X0NWR5 | Trypanosomatidae | 51% | 100% |
A0A1X0P4M9 | Trypanosomatidae | 38% | 100% |
A0A3R7JY84 | Trypanosoma rangeli | 51% | 100% |
A0A3R7N130 | Trypanosoma rangeli | 41% | 96% |
A0A3S7WRP1 | Leishmania donovani | 90% | 100% |
A0A3S7X742 | Leishmania donovani | 43% | 100% |
A1K9L5 | Azoarcus sp. (strain BH72) | 32% | 100% |
A1VP99 | Polaromonas naphthalenivorans (strain CJ2) | 29% | 100% |
A2SH61 | Methylibium petroleiphilum (strain ATCC BAA-1232 / LMG 22953 / PM1) | 32% | 100% |
A4H6I8 | Leishmania braziliensis | 84% | 100% |
A4HCW4 | Leishmania braziliensis | 34% | 100% |
A4HLW7 | Leishmania braziliensis | 44% | 97% |
A4HUX3 | Leishmania infantum | 90% | 100% |
A4I996 | Leishmania infantum | 43% | 100% |
A6X259 | Brucella anthropi (strain ATCC 49188 / DSM 6882 / CCUG 24695 / JCM 21032 / LMG 3331 / NBRC 15819 / NCTC 12168 / Alc 37) | 30% | 100% |
A9IIK3 | Bordetella petrii (strain ATCC BAA-461 / DSM 12804 / CCUG 43448) | 32% | 100% |
B1LVC3 | Methylobacterium radiotolerans (strain ATCC 27329 / DSM 1819 / JCM 2831 / NBRC 15690 / NCIMB 10815 / 0-1) | 30% | 100% |
B1V932 | Phytoplasma australiense | 32% | 100% |
B2FMS4 | Stenotrophomonas maltophilia (strain K279a) | 30% | 100% |
B4SJ73 | Stenotrophomonas maltophilia (strain R551-3) | 30% | 100% |
B5EKZ2 | Acidithiobacillus ferrooxidans (strain ATCC 53993 / BNL-5-31) | 31% | 100% |
B7J5I9 | Acidithiobacillus ferrooxidans (strain ATCC 23270 / DSM 14882 / CIP 104768 / NCIMB 8455) | 31% | 100% |
B8D7Q4 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain Tuc7) | 30% | 100% |
B8D9F2 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain 5A) | 30% | 100% |
B8HTK3 | Cyanothece sp. (strain PCC 7425 / ATCC 29141) | 27% | 100% |
C1F4B7 | Acidobacterium capsulatum (strain ATCC 51196 / DSM 11244 / BCRC 80197 / JCM 7670 / NBRC 15755 / NCIMB 13165 / 161) | 31% | 100% |
C3K6G5 | Pseudomonas fluorescens (strain SBW25) | 33% | 100% |
C3M9C8 | Sinorhizobium fredii (strain NBRC 101917 / NGR234) | 30% | 100% |
C4K346 | Hamiltonella defensa subsp. Acyrthosiphon pisum (strain 5AT) | 31% | 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) | 34% | 100% |
C6E543 | Geobacter sp. (strain M21) | 33% | 100% |
D0A654 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 95% |
D0A7H3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9B496 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
P28838 | Homo sapiens | 27% | 100% |
P57448 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) | 30% | 100% |
P57823 | Pasteurella multocida (strain Pm70) | 32% | 100% |
Q0SQ50 | Clostridium perfringens (strain SM101 / Type A) | 26% | 100% |
Q1LJJ6 | Cupriavidus metallidurans (strain ATCC 43123 / DSM 2839 / NBRC 102507 / CH34) | 31% | 100% |
Q2KWX0 | Bordetella avium (strain 197N) | 30% | 100% |
Q2YB18 | Nitrosospira multiformis (strain ATCC 25196 / NCIMB 11849 / C 71) | 31% | 100% |
Q315M7 | Oleidesulfovibrio alaskensis (strain ATCC BAA-1058 / DSM 17464 / G20) | 28% | 100% |
Q3A831 | Syntrophotalea carbinolica (strain DSM 2380 / NBRC 103641 / GraBd1) | 32% | 100% |
Q46XT9 | Cupriavidus pinatubonensis (strain JMP 134 / LMG 1197) | 32% | 100% |
Q4Q3T0 | Leishmania major | 43% | 97% |
Q4QH17 | Leishmania major | 89% | 100% |
Q5FFZ5 | Ehrlichia ruminantium (strain Gardel) | 30% | 100% |
Q5HAP2 | Ehrlichia ruminantium (strain Welgevonden) | 30% | 100% |
Q5QY05 | Idiomarina loihiensis (strain ATCC BAA-735 / DSM 15497 / L2-TR) | 29% | 100% |
Q5R7G6 | Pongo abelii | 37% | 100% |
Q68XM6 | Rickettsia typhi (strain ATCC VR-144 / Wilmington) | 32% | 100% |
Q6NSR8 | Mus musculus | 39% | 100% |
Q73QZ3 | Treponema denticola (strain ATCC 35405 / DSM 14222 / CIP 103919 / JCM 8153 / KCTC 15104) | 30% | 100% |
Q73YK2 | Mycolicibacterium paratuberculosis (strain ATCC BAA-968 / K-10) | 31% | 100% |
Q7M8W6 | Wolinella succinogenes (strain ATCC 29543 / DSM 1740 / LMG 7466 / NCTC 11488 / FDC 602W) | 33% | 100% |
Q7W5K6 | Bordetella parapertussis (strain 12822 / ATCC BAA-587 / NCTC 13253) | 31% | 100% |
Q89AG2 | Buchnera aphidicola subsp. Baizongia pistaciae (strain Bp) | 28% | 100% |
Q8D295 | Wigglesworthia glossinidia brevipalpis | 28% | 100% |
Q8K9I0 | Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) | 30% | 100% |
Q8NDH3 | Homo sapiens | 37% | 100% |
Q8SQZ7 | Encephalitozoon cuniculi (strain GB-M1) | 29% | 100% |
Q8XHI3 | Clostridium perfringens (strain 13 / Type A) | 27% | 100% |
Q984S1 | Mesorhizobium japonicum (strain LMG 29417 / CECT 9101 / MAFF 303099) | 30% | 100% |
Q9JTI8 | Neisseria meningitidis serogroup A / serotype 4A (strain DSM 15465 / Z2491) | 32% | 100% |
Q9KTX5 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 31% | 100% |
V5BTR1 | Trypanosoma cruzi | 41% | 96% |
V5BWE3 | Trypanosoma cruzi | 49% | 100% |