Alignments for a candidate for xacD in Hippea jasoniae Mar08-272r

GapMind for catabolism of small carbon sources

Alignments for a candidate for xacD in Hippea jasoniae Mar08-272r

Align L-arabonate dehydratase (EC 4.2.1.25) (characterized)
to candidate WP_035586458.1 EK17_RS00375 dihydroxy-acid dehydratase

Query= reanno::Smeli:SM_b20890
         (579 letters)



>NCBI__GCF_000744435.1:WP_035586458.1
          Length = 555

 Score =  370 bits (950), Expect = e-107
 Identities = 220/553 (39%), Positives = 319/553 (57%), Gaps = 16/553 (2%)

Query: 21  GKNAIMHRSWMKNQGLPADTFDGRPIIGICNTWSELTPCNAHLRDLAERVKRGVYEAGGF 80
           G     HRS  K  G   D    RPII I N+++ + P + H++ L E VK G+Y AGG 
Sbjct: 11  GPQRAPHRSLFKADGY-TDIELNRPIIAIANSYNTIVPGHVHMQQLVEAVKYGIYMAGGT 69

Query: 81  PVEFPVFSTGESTLRPTAMMF-----RNLAAMDVEESIRGNPVDGVVLLGGCDKTTPSLL 135
           P+EF V    +        M      R L A  VE  +  +PVDG+V+L  CDK  P ++
Sbjct: 70  PIEFNVIGVDDGIAMGHLGMHYSLPSRELIADSVETMVNAHPVDGLVILPACDKIVPGMM 129

Query: 136 MGAASVDIPAIVVSGGPMLNGKWRGKDVGSGTAIWQFSEMVKSGEMSLEEFMDAEQGMAR 195
           M AA V+IPAI++SGGPML G++ G D+          + V +GE++ EE    E+    
Sbjct: 130 MAAARVNIPAIMISGGPMLAGRFSGTDIDLAQVFEAVGKYV-NGEITEEELRAVEEAGCP 188

Query: 196 SAGSCMTMGTASTMASMAEALGMTLSGNAAIPAVDARRRVISQLTGRRIVEMVKEDLKPS 255
           S GSC  M +A+++  ++E LG++L GN  IPA  A R  +++L G +IVE+V++ +KP 
Sbjct: 189 SCGSCSGMYSANSINCISEVLGLSLPGNGTIPAPMAARVRLAKLAGMKIVELVEKGIKPR 248

Query: 256 DILTKEAFENAIRVNGAVGGSTNAVLHLLALAGRVGVDLSLDDWDRLGRDVPTIVNLQPS 315
           DI+TKEAF NAI  + A+G STN VLHLLA+A    VDL+LDD+D+L   VP +    P 
Sbjct: 249 DIMTKEAFLNAIVADMAMGCSTNTVLHLLAIANEAEVDLTLDDFDKLTDKVPDLCAFSPV 308

Query: 316 GKYLMEEFYYAGGLPVVIKAVAEMGLLHNDAITVSGDTIWNDVKGVVNYNEDVILPREKA 375
           G Y +++   AGG+  ++  +  +GLL++D ITVSG TI+ + K    Y ++VI P +K 
Sbjct: 309 GPYHLQDLDEAGGMMALLNRLEPLGLLNHDCITVSGKTIYENYKNARVYRDEVIRPLDKP 368

Query: 376 LTKSGGIAVLRGNLAPRGAVLKPSAASPHLMQHKGRAVVFESIEDYHARINREDLDIDET 435
               GG+ +L+GNLAP GAVLK S     + +  GRA VF+S E+    I  +  DI + 
Sbjct: 369 YFPRGGLTILKGNLAPDGAVLKQSGVDVSMNKFVGRARVFDSEEEALKAIFAK--DIHKG 426

Query: 436 CIMVLKYCGPKGYPGMAEVGNMGLPPKVLKKGI---TDMIRISDARMSGTAYGTVILHTA 492
            ++V++Y GP G PGM E+    L P     G+    D+  I+D R SG   G  + H A
Sbjct: 427 DVVVIRYEGPAGGPGMKEM----LQPTSAIAGMGLDKDVALITDGRFSGATRGLSVGHIA 482

Query: 493 PEAAEGGPLALVENGDLIEVDIPNRTLHLHVSDEELARRRAAWVSPVKPLTGGYGGLYIK 552
           PEAA GG + L+E GD IE D+ N+T++L V ++ + +RR  +      +T G+   Y K
Sbjct: 483 PEAARGGLIGLIEEGDKIEFDVENKTMNLLVDEKTIEQRRKNFKPKPPKITKGWLARYAK 542

Query: 553 TVMQADAGADLDF 565
            V  A  GA L++
Sbjct: 543 MVGSAAKGAVLEY 555


Lambda     K      H
   0.318    0.135    0.402 

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: 846
Number of extensions: 40
Number of successful extensions: 5
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: 579
Length of database: 555
Length adjustment: 36
Effective length of query: 543
Effective length of database: 519
Effective search space:   281817
Effective search space used:   281817
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 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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Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
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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