Alignments for a candidate for ARO8 in Paraburkholderia bryophila 376MFSha3.1

GapMind for catabolism of small carbon sources

Alignments for a candidate for ARO8 in Paraburkholderia bryophila 376MFSha3.1

Align Bifunctional aspartate aminotransferase and L-aspartate beta-decarboxylase; Aspartate 4-decarboxylase; Asd; AsdP; EC 2.6.1.1; EC 4.1.1.12 (characterized)
to candidate H281DRAFT_04749 H281DRAFT_04749 aspartate 4-decarboxylase

Query= SwissProt::Q53IZ1
         (531 letters)



>FitnessBrowser__Burk376:H281DRAFT_04749
          Length = 554

 Score =  616 bits (1589), Expect = 0.0
 Identities = 315/526 (59%), Positives = 388/526 (73%), Gaps = 7/526 (1%)

Query: 8   LANLSPFELKDELIKVASG-----KANRLMLNAGRGNPNFLATTPRRAFFRLGLFAAAES 62
           LA LSPFELKDELIK A G      AN  MLNAGRGNPNFLAT PR  F++LGLFA  ES
Sbjct: 18  LAALSPFELKDELIKAAGGGAVERPANASMLNAGRGNPNFLATIPRHGFWQLGLFAMRES 77

Query: 63  ELSYSYMTVGVGGLAKLDGIEGRFERFIAEHRDQEGVKFLGKSLSYVRDQLGLDPAAFLH 122
           E S++YM  GVGG  + +G+E RF+ F+ E++   G+ FL  ++SYVRDQLGL    FL+
Sbjct: 78  ERSFAYMPEGVGGFPRREGLEERFDLFLRENKGVAGIDFLRGAVSYVRDQLGLSAGDFLY 137

Query: 123 EMVDGILGCNYPVPPRMLTVSEQIVRQYIVREMAGGAVPPESVDLFAVEGGTAAMAYIFE 182
           EM +GILG NYPVP RML +SE IV QY+ REM G        D+FAVEGGTAAM YIF 
Sbjct: 138 EMCEGILGSNYPVPDRMLKLSEVIVGQYLRREMIGRHPFVGEFDVFAVEGGTAAMTYIFN 197

Query: 183 SLRISGLLKAGDKVAIGMPVFTPYIEIPELAQYDLKEVPIHADPDNGWQYSDAELDKLKD 242
           ++R + L+K GD +A+GMP+FTPYIEIP L  Y L  V ++A  +NGWQY+  ELDKL+D
Sbjct: 198 TMRENHLIKPGDTIALGMPIFTPYIEIPRLNDYQLNVVNLNAGVENGWQYTKEELDKLRD 257

Query: 243 PDVKIFFCVNPSNPPSVKMDQRSLDRVRAIVAEQRPDLLILTDDVYGTFADEFQSLFSVC 302
           P VK FF VNPSNPPSVKMD  SL  +  IV E RPDL++LTDDVYGTFAD+F SLF++ 
Sbjct: 258 PKVKAFFLVNPSNPPSVKMDDESLQYIADIVKE-RPDLILLTDDVYGTFADDFVSLFALA 316

Query: 303 PRNTLLVYSFSKYFGATGWRLGVIAAHKDNVFDHALSQLPESAKKALDHRYRSLLPDVRS 362
           P+NT+LVYS+SKYFGATGWRLG IA H+DNV D  +S+LP+  KK L  RY S+  +   
Sbjct: 317 PKNTILVYSYSKYFGATGWRLGTIATHRDNVLDRLISELPKDVKKQLHERYESITTEPEK 376

Query: 363 LKFIDRLVADSRVVALNHTAGLSTPQQVQMVLFSLFALMDEADAYKQALKQLIRRREATL 422
           LKFIDRLVADSR VALNHTAGLSTPQQVQMVLFSLF+LMD  DAYK ALK+LIR+R+  L
Sbjct: 377 LKFIDRLVADSRTVALNHTAGLSTPQQVQMVLFSLFSLMDTPDAYKNALKRLIRKRKQAL 436

Query: 423 YRELGMP-PLENPNSVNYYTLIDLQNVTCRLYGEAFSQWAVQQSSTGDMLFRVADETGIV 481
           Y E+G+     +PN V+YYT++D + +  R++G  F  W ++ +   ++LFR+A E  +V
Sbjct: 437 YEEVGIAFDDSDPNQVDYYTILDAEYLGERMFGREFVDWQLKSTQPTELLFRLAREARVV 496

Query: 482 LLPGRGFGSDRPSGRASLANLNEYEYAAIGRALRRLADELYEQYKA 527
           LLPG GFG+   SGR SLANLNE +Y  IGRA+RRL +E  E++ A
Sbjct: 497 LLPGLGFGTQHASGRVSLANLNESDYRQIGRAVRRLIEEYVERFNA 542


Lambda     K      H
   0.321    0.138    0.400 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 809
Number of extensions: 33
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 531
Length of database: 554
Length adjustment: 35
Effective length of query: 496
Effective length of database: 519
Effective search space:   257424
Effective search space used:   257424
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Protein sequences (fasta format)
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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

the paper from 2019 on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory

GapMind for catabolism of small carbon sources