Aligments for a candidate for xacF in Dinoroseobacter shibae DFL-12

GapMind for catabolism of small carbon sources

Aligments for a candidate for xacF in Dinoroseobacter shibae DFL-12

Align Alpha-ketoglutaric semialdehyde dehydrogenase 2; alphaKGSA dehydrogenase 2; 2,5-dioxovalerate dehydrogenase 2; KGSADH-II; EC 1.2.1.26 (characterized)
to candidate 3609053 Dshi_2442 aldehyde dehydrogenase (RefSeq)

Query= SwissProt::Q08IC0
         (525 letters)



>lcl|FitnessBrowser__Dino:3609053 Dshi_2442 aldehyde dehydrogenase
           (RefSeq)
          Length = 501

 Score =  495 bits (1274), Expect = e-144
 Identities = 275/501 (54%), Positives = 332/501 (66%), Gaps = 9/501 (1%)

Query: 5   GEMLIGAEAVAGSAGTLRAFDPSKGEPIDAPVFGVAAQADVERACELARDAFDAYRAQPL 64
           G+ LI A A  GS  T  A DP+ G    A  F V   A V++AC  A DAF +Y     
Sbjct: 7   GKHLI-AGAWVGSDQTF-ASDPAHGP---AHEFSVGTPALVDQACAAAEDAFASYGYSDA 61

Query: 65  AARAAFLEAIADEIVALGDALIERAHAETGLPVARLQGERGRTVGQLRLFARVVRDGRFL 124
           A RAAFL AIADEI A    +      ETGLP ARLQGERGRT GQLRLFA  +  G  L
Sbjct: 62  ATRAAFLNAIADEIDARAQIITGIGTQETGLPEARLQGERGRTTGQLRLFAEHILKGDCL 121

Query: 125 AASIDPAQPARTPLPRSDLRLQKVGLGPVVVFGASNFPLAFSVAGGDTASALAAGCPVIV 184
               DPA P R PLPR DL+L +  +GPV VFGASNFPLAFSVAGGDTA+ALAAGCPV+V
Sbjct: 122 DRRHDPALPDRAPLPRPDLKLVQRPIGPVAVFGASNFPLAFSVAGGDTAAALAAGCPVVV 181

Query: 185 KAHEAHLGTSELVGRAIRAAVAKTGMPAGVFSLLVGPGRVIGGALVSHPAVQAVGFTGSR 244
           K H AH GT E+V  AI AA+A+TGMPAGVFSL+ G  R +G ALV HP ++AVGFTGS 
Sbjct: 182 KGHSAHPGTGEIVAEAIHAAIARTGMPAGVFSLIQGGKRDVGTALVQHPLIRAVGFTGSL 241

Query: 245 QGGMALVQIANARPQPIPVYAEMSSINPVVLFPAALAARGDAIATGFVDSLTLGVGQFCT 304
            GG AL  +  ARP+PIP + E+ S+NP+ L P A+AARG  I  G+  SL +G GQFCT
Sbjct: 242 AGGRALFDLCAARPEPIPFFGELGSVNPMFLLPEAIAARGAEIGAGWAGSLAMGAGQFCT 301

Query: 305 NPGLVLAIDGPDLDRFETVAAQALAKKPAGVMLTQGIADAYRNGRGKLAELPGVREIGAG 364
           NPG+ + +  P  D F   A  AL +  A  MLT+GIA AYR+G  +LA  P   E+   
Sbjct: 302 NPGIAVVL--PGADAFVAAAEAALRETAAQTMLTEGIAAAYRDGVARLAAHPQTSELLG- 358

Query: 365 EAAQTDCQAGGALYEVGAQAFLAEPAFSHEVFGPASLIVRCRDLDEVARVLEALEGQLTA 424
            A     +A   LY V A+ +LA+     EVFGP  L+V  +D  E+AR+  +L+GQLT 
Sbjct: 359 -APCDGREAHPCLYRVAARDWLADHTLQEEVFGPLGLVVEAQDAAEMARIARSLQGQLTC 417

Query: 425 TLQMDADDKPLARRLLPVLERKAGRLLVNGYPTGVEVCDAMVHGGPFPATSNPAVTSVGA 484
           TL M+  D   AR L+P+LERKAGR+LVNG+PTGVEV D+MVHGGP+PA++N   TSVG 
Sbjct: 418 TLHMEDGDTDHARSLVPLLERKAGRMLVNGFPTGVEVADSMVHGGPYPASTNFGATSVGT 477

Query: 485 TAIERFLRPVCYQDFPDDLLP 505
            +I RFLRPVCYQ+ PD LLP
Sbjct: 478 LSIRRFLRPVCYQNMPDALLP 498


Lambda     K      H
   0.320    0.137    0.396 

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: 914
Number of extensions: 44
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: 525
Length of database: 501
Length adjustment: 35
Effective length of query: 490
Effective length of database: 466
Effective search space:   228340
Effective search space used:   228340
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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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, or view the source code.

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