Alignments for a candidate for xacD in Alkalitalea saponilacus SC/BZ-SP2

GapMind for catabolism of small carbon sources

Alignments for a candidate for xacD in Alkalitalea saponilacus SC/BZ-SP2

Align L-arabonate dehydratase; L-arabinonate dehydratase; EC 4.2.1.25 (characterized)
to candidate WP_079558836.1 CDL62_RS07395 dihydroxy-acid dehydratase

Query= SwissProt::Q1JUQ1
         (583 letters)



>NCBI__GCF_002201795.1:WP_079558836.1
          Length = 613

 Score =  249 bits (635), Expect = 3e-70
 Identities = 175/562 (31%), Positives = 280/562 (49%), Gaps = 63/562 (11%)

Query: 25  RSWMKNQGIPDHEFDGRPIIGICNTWSELTPCNAHFRKLAEHVKRGISEAGGFPVEFPVF 84
           RS  +  G+ D +  GRP+I + N++++  P +AH  ++ + VKR I + G F  EF   
Sbjct: 20  RSLWRANGMKDEQM-GRPLIAVVNSFTQFVPGHAHLHQIGQDVKRMIEKQGCFAAEFNTI 78

Query: 85  SNGES-NLRPSAML----TRNLASMDVEEAIRGNPIDAVVLLAGCDKTTPALLMGAASCD 139
           +  +   +    ML    +R+L +  VE  +  +  DA+V ++ CDK TP +LM A   +
Sbjct: 79  AIDDGIAMGHDGMLYSLPSRDLIADSVEYMVNAHQADAMVCISNCDKITPGMLMAAMRIN 138

Query: 140 VPAIVVSGGPMLNGKLEGKNIGSGTAVWQLHEALKAGEIDVHHFLSAEAGMSRSAGTCNT 199
           +P I VSGGPM  GK+  K +    ++    +   + E      L+ E     + G+C+ 
Sbjct: 139 IPVIFVSGGPMEAGKVGDKALDLVDSMVMAADDSVSDE----ELLAVEQNACPTCGSCSG 194

Query: 200 MGTASTMACMAEALGVALPHNAAIPAVDSRRYVLAHMSGIRIVEMAL-------EGLVLS 252
           M TA++M C+ EALG+ALP N  I A    R  L   +  +IV +A        E ++  
Sbjct: 195 MFTANSMNCLNEALGLALPGNGTIVATHVNRKKLFEKAANQIVRLAYKYYQDGDESVLPR 254

Query: 253 KILTRAAFENAIRANAAIGGSTNAVIHLKAIAGRIGVPLELEDWMRIGRDTPTIVDLMPS 312
            I T+AAF N++  + A+GGSTN V+HL AIA   GV   ++D  RI R TP +  + P+
Sbjct: 255 NIATKAAFNNSMTLDVAMGGSTNTVLHLLAIAHEAGVDFTMQDIDRISRKTPVLCKVAPN 314

Query: 313 GRFPMEEFYYAGGLPAVLRRLGEGGLLPNP-------------DALTVNGKSLWDNVRE- 358
             + +E+   AGG+  +L  L  GGLL                DA  +  KS     +E 
Sbjct: 315 SDYHIEDVNRAGGIMGILAELNRGGLLDATVGRVDYSSLSEALDAYDMASKSAIAEAKEI 374

Query: 359 ---AP--------------------NYDEEVIRPLDRPLIADGGIRILRGNLAPRGAVLK 395
              AP                    + ++  IR +      DGG+ +L GN+A  G ++K
Sbjct: 375 YQSAPGGFVNLVMGSQKAIYGELDLDREKGCIRNISHAYSQDGGLAVLFGNIAENGCIVK 434

Query: 396 PSAASPELLKHRGRAVVFENLDHYKATINDEALDIDASSVMVLKNCGPRGYPGMAEVGNM 455
            +     +    G A V+E+ D   A     + ++ A  V+++K  GP+G PGM E   M
Sbjct: 435 TAGVDESIFHFEGTARVYESQDD--ACDGILSGEVKAGDVVIIKYEGPKGGPGMQE---M 489

Query: 456 GLPPKLLRQ---GVKDMVRISDARMSGTAYGTVVLHVAPEAAAGGPLAAVRNGDWIELDC 512
             P   L+    G K  + ++D R SG   G  + H +PEAAAGG +A ++NGD + +D 
Sbjct: 490 LYPTSYLKSRNLGAKCAL-LTDGRFSGGTSGLSIGHASPEAAAGGAIALIKNGDKVIIDI 548

Query: 513 EAGTLHLDITDDELHRRLSDVD 534
              ++++D+T+DEL++R +  D
Sbjct: 549 PQRSINIDVTEDELNQRRAAED 570


Lambda     K      H
   0.319    0.136    0.412 

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: 874
Number of extensions: 53
Number of successful extensions: 7
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 583
Length of database: 613
Length adjustment: 37
Effective length of query: 546
Effective length of database: 576
Effective search space:   314496
Effective search space used:   314496
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 (21.7 bits)
S2: 53 (25.0 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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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 2024 update 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