Alignments for a candidate for mmsA in Cereibacter sphaeroides ATCC 17029

GapMind for catabolism of small carbon sources

Alignments for a candidate for mmsA in Cereibacter sphaeroides ATCC 17029

Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_011842384.1 RSPH17029_RS17490 aldehyde dehydrogenase family protein

Query= reanno::pseudo5_N2C3_1:AO356_23175
         (500 letters)



>NCBI__GCF_000015985.1:WP_011842384.1
          Length = 791

 Score =  234 bits (597), Expect = 8e-66
 Identities = 156/493 (31%), Positives = 244/493 (49%), Gaps = 22/493 (4%)

Query: 7   VGHYIDGRIQASDNARLSNVFNPATGAVQARVALAEPSTVDAAVASALAAFPAWSEQSSL 66
           +GHYIDG    ++ A +  V NPATG + AR+  A  + ++AAVA+A AAF  WS+    
Sbjct: 33  LGHYIDGAFTGAETAAIE-VENPATGEILARIPAAGEAEIEAAVAAARAAFSGWSQLPGF 91

Query: 67  RRSRVMFKFKELLDRHHDELAQIISREHGKVLSDAH-GEVTRGIEIVEYACGAPNLLKTD 125
            R+R ++     L +     + + + ++GK + +    +V   I    +  G   +L  +
Sbjct: 92  ERARYLYAIARGLQKRERFFSVLETLDNGKAIRETRTADVPLAIRHFYHHAGWAAVLGEE 151

Query: 126 FSDNIGGGIDNWNLRQPLGVCAGVTPFNFPVMVPLWMIPLALVAGNCFILKPSERDPSAS 185
           F  +           +PLGVC  V P+NFP+++  W I  AL AGN  +LKP++  P  +
Sbjct: 152 FPGH-----------EPLGVCGQVIPWNFPMLMLAWKIAPALAAGNTVVLKPADLTPLTA 200

Query: 186 LLMARLLTEAGLPDGVFNVVQGDKVAVDALLQHPDIEAISFVGSTPIAEYIHQQGTAQGK 245
           +  A +L E GLP GV N+V G       L++HP +  ++F GST +   I +     GK
Sbjct: 201 VAFAEMLDEIGLPRGVVNIVHGGAETGALLVRHPGVAKVAFTGSTAVGREIRRATAGSGK 260

Query: 246 RVQALGGAKNHMIVMPDADLDQAADALIGAAYGSAGERCMAISIAVAVGDVGDELIAKLL 305
            +    G K+  +V  DADLD A + ++   + + GE C A S  +    + +  +AKL 
Sbjct: 261 SLTLELGGKSPFVVCADADLDAAVEGVVEGVWFNQGEVCCAGSRLLLQEGIAERFLAKLR 320

Query: 306 PRIDQLKIGNGQQPGTDMGPLVTAEHKAKVEGFIDAGVAEGARLIVDGRGFKVPGAEQGF 365
            R++++++G+     TDMG +V+A  KA++E  I     EG RL  +     +P A  G 
Sbjct: 321 ARMEKIRVGDPLDKSTDMGAIVSARQKARIEELIAGAAREGYRL--EQAACPLPAA--GH 376

Query: 366 FVGATLFDQVTAEMSIYQQEIFGPVLGIVRVPDFATAVALINAHEFGNGVSCFTRDGGIA 425
           FV    F       ++ Q EIFGP+           AVAL N   +G   S ++ +   A
Sbjct: 377 FVAPGFFADTEPAATVAQVEIFGPIAVTTTFRTVDEAVALANNTPYGLAASVWSENINAA 436

Query: 426 RAFARSIKVGMVGINVPIPVPMAWHSFGGWKRSLFGDHHAYGEEGLRFYSRYKSVMQRWP 485
              A  I+ G+V IN    +  A  SFGG K S FG   A   EGL  Y R ++   R P
Sbjct: 437 TELAARIRAGVVWINAS-NLFDAGASFGGMKESGFGREGA--REGLGAYLRPRT--PRGP 491

Query: 486 DSIAKGPEFSMPT 498
           +++    +F+  T
Sbjct: 492 EALVAPVDFTAHT 504



 Score = 53.9 bits (128), Expect = 2e-11
 Identities = 60/252 (23%), Positives = 102/252 (40%), Gaps = 20/252 (7%)

Query: 9   HYIDGRIQASDNARLSNVFNPATGAVQARVALAEPSTVDAAVASALAAFPAWSEQSSLRR 68
           +YI G  Q   +   S V     G       ++    +  AV +AL A   W+  +  R 
Sbjct: 520 NYIGGA-QVRPDGGASYVVRGPKGEALGLAPVSGRKDIRNAVEAALKA-KGWAANAHGRA 577

Query: 69  SRVMFKFKELLDRHHDELAQIISREHGKVLSDAHGEVTRGIEIVEYACGAPNLLKTDFSD 128
             + F  + +  R  D  A ++    G+  S+A  EV   IE V +  G         +D
Sbjct: 578 QVLFFLAENIAARAEDLAAALVQGGAGR--SEAAAEVRSLIERVFFYAG--------MAD 627

Query: 129 NIGGGID-------NWNLRQPLGVCAGVTPFNFPVMVPLWMIPLALVAGNCFILKPSERD 181
              G I          ++++PLGV   + P   P++  + +I   + AGN  +  PS   
Sbjct: 628 KDDGRIHATKPRHLTLSVKEPLGVVGVLAPDEAPLLSLMSLILPLIAAGNRVVAVPSPAQ 687

Query: 182 PSASLLMARLLTEAGLPDGVFNVVQGDK-VAVDALLQHPDIEAISFVGSTPIAEYIHQQG 240
              +  + ++   + LP GV N+V GD+ +    L +H  ++ I + GS   A  +    
Sbjct: 688 ALLAQPLTQIFDTSDLPGGVVNLVTGDRNLLARTLAEHDAVDGIWYHGSAKGAAEVEALS 747

Query: 241 TAQGKRVQALGG 252
               K+V   GG
Sbjct: 748 AGNLKQVWTNGG 759


Lambda     K      H
   0.320    0.137    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: 910
Number of extensions: 42
Number of successful extensions: 6
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 500
Length of database: 791
Length adjustment: 38
Effective length of query: 462
Effective length of database: 753
Effective search space:   347886
Effective search space used:   347886
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: 54 (25.4 bits)

This GapMind analysis is from Apr 10 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:

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