GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mmsA in Erythrobacter gangjinensis K7-2

Align methylmalonate-semialdehyde dehydrogenase (CoA-acylating) (EC 1.2.1.27) (characterized)
to candidate WP_047007470.1 AAW01_RS11975 succinylglutamate-semialdehyde dehydrogenase

Query= BRENDA::P42412
         (487 letters)



>NCBI__GCF_001010925.1:WP_047007470.1
          Length = 481

 Score =  161 bits (408), Expect = 4e-44
 Identities = 120/410 (29%), Positives = 188/410 (45%), Gaps = 6/410 (1%)

Query: 45  DIDYAAQTAAEAFKTWSKVAVPRRARILFNFQQLLSQHKEELAHLITIENGKNTKEALGE 104
           ++D     A +A+  W+   + +R  ++  F   +   ++E A LI+ E GK   EA  E
Sbjct: 34  NVDEYVARARKAWPGWAAEPLAKRIELVRRFVNEVRAEQDEFAQLISRETGKPLWEARTE 93

Query: 105 VGRGIENVEFAAGAPSLMMGDSLASIATDVEAANYRYPIGVVGGIAPFNFPMMVPCWMFP 164
           V   +  V+ +  A +   G      A    AA    P GV+  + P+NFP  +P     
Sbjct: 94  VEAVMAKVDISITAYAERTGQRKLDSALQGSAALRHKPHGVMAVLGPYNFPAHLPNGHIV 153

Query: 165 MAIALGNTFILKPSERTPLLTEKLVELFEKAGLPKGVFNVVYGAHDVVNGILEHPEIKAI 224
            A+  GN  ILKPSE+TP + E+L+  F KAG+P+ V   + G  D    ++ H ++  +
Sbjct: 154 PALIAGNAIILKPSEKTPAVGERLLSFFHKAGIPQDVVQCLIGGPDEGKALVAHADVDGV 213

Query: 225 SFVGSKPVGEYVYKKGSENLKRVQSLTGAKNHTIVLNDA-NLEDTVTNIVGAAFGSAGER 283
            F GS  VG  + +K + N  ++ +L    N+ IVL D   LED    I+ +AF +AG+R
Sbjct: 214 LFTGSAQVGIAINRKLASNPGKMVALEMGGNNPIVLWDTPKLEDAAALIIQSAFTTAGQR 273

Query: 284 CMACAVVTVEEGIADEFMAKLQEKVADIKIGNGL-DDGVFLGPVIREDNKKRTLSYIEKG 342
           C A   + V+  + D  +  + +    + +     D   F+GPVI      +        
Sbjct: 274 CTAGRRLIVKSSMYDAALEAVTKLTDRLLVDEPFADPAPFMGPVIDNQTADQLTESFLYL 333

Query: 343 LEEGARLVCDGRENVSDDGYFVGPTIFDNVTTEMTIWKD-EIFAPVLSVIRVKNLKEAIE 401
           L  G + +   R     D  F+ P+I D  TT M    D E+F P+L V+RV +   AI 
Sbjct: 334 LSNGGKAIKHLR-RPHGDLPFLSPSIID--TTNMAERPDVELFGPILQVVRVDDFDAAIA 390

Query: 402 IANKSEFANGACLFTSNSNAIRYFRENIDAGMLGINLGVPAPMAFFPFSG 451
            AN + F   A L   +      F  NI AG++  N       +  PF G
Sbjct: 391 EANNTRFGLSASLIGGDPKQYNRFWANIRAGIVNWNRPTNGASSAAPFGG 440


Lambda     K      H
   0.318    0.136    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: 504
Number of extensions: 23
Number of successful extensions: 3
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: 487
Length of database: 481
Length adjustment: 34
Effective length of query: 453
Effective length of database: 447
Effective search space:   202491
Effective search space used:   202491
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 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:

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