GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gabD in Chlorobium phaeobacteroides BS1

Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate 642684612 Cphamn1_2121 Aldehyde Dehydrogenase

Query= BRENDA::P23883
         (495 letters)



>IMG__ChlphaBS1_FD:642684612
          Length = 469

 Score =  135 bits (339), Expect = 4e-36
 Identities = 101/340 (29%), Positives = 169/340 (49%), Gaps = 14/340 (4%)

Query: 155 REPVGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKPSEKSP-LSAIRLAGLAKEAGLP 213
           REP GV+  +  WN+PL L       A+AAGN V++KPSE+SP  S + + G+ +   L 
Sbjct: 111 REPYGVVLVVAAWNYPLQLAVAPAIGAIAAGNCVMIKPSEQSPATSELLVEGVGRY--LD 168

Query: 214 DGVLNVVTGFGHEAGQALSRHNDIDAIAFTGSTRTGKQLLKDAGDSNMKRVWLEAGGKSA 273
              + V  G   E+ Q L      D I FTG  +TGKQ+++ A + ++  V LE GGK+ 
Sbjct: 169 GKAIKVFPGGVEESRQLL--EESFDYIFFTGGIKTGKQVMRKAAE-HLTPVSLELGGKNP 225

Query: 274 NIVFADCPDLQQAASATAAGIFYNQGQVCIAGTRLLLEESIADEFLALLKQQAQNWQPGH 333
            IV  +  ++  AA       F N GQ CIA   +L++ +  +E L  +K   + +    
Sbjct: 226 CIVDQN-TNIPVAARRIVWAKFLNAGQTCIAPDYVLVDRNAEEELLRCMKDAVEAFYGTE 284

Query: 334 PLDPATTMGTLIDCAHADSVHSFIREGESKGQLLLDGRNAGLAAAIGPTIFVDVDPNASL 393
           P + +     +I  A  + +  ++ E    G ++  G        + PTI  +V P+A +
Sbjct: 285 P-EESLDYPAVITEARLEKLAGYLDE----GIVVTGGSTDAGRRYLSPTILREVSPDARV 339

Query: 394 SREEIFGPVLVVTRFTSEEQALQLANDSQYGLGAAVWTRDLSRAHRMSRRLKAGSVFVNN 453
             +EIFGPVL V  + + E AL++   +++ L   V++ D S    M +  ++G V +N+
Sbjct: 340 MTDEIFGPVLPVLSYETPEDALRVVRMARHPLALYVFSGDRSFQEYMIQNTQSGGVCIND 399

Query: 454 --YNDGDMTVPFGGYKQSGNGRDKSLHALEKFTELKTIWI 491
             +      +PFGG  +SG G        E F+  +++ +
Sbjct: 400 LMFQAAIPALPFGGAGESGMGVYHGAAGFETFSRPRSVHV 439


Lambda     K      H
   0.317    0.133    0.389 

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: 479
Number of extensions: 27
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: 495
Length of database: 469
Length adjustment: 34
Effective length of query: 461
Effective length of database: 435
Effective search space:   200535
Effective search space used:   200535
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: 52 (24.6 bits)

This GapMind analysis is from Apr 09 2024. 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:

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:

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:

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:

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