GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serA in Methanosarcina acetivorans C2A

Align D-3-phosphoglycerate dehydrogenase; PGDH; EC 1.1.1.95 (uncharacterized)
to candidate WP_011021352.1 MA_RS06920 glycerate dehydrogenase

Query= curated2:O27051
         (525 letters)



>NCBI__GCF_000007345.1:WP_011021352.1
          Length = 319

 Score =  242 bits (617), Expect = 2e-68
 Identities = 138/319 (43%), Positives = 201/319 (63%), Gaps = 7/319 (2%)

Query: 4   MKVLIADSI--NEKGISELEEVAEVVV--NTTITPEELLDAIKDFDAIVVRSRTKVTREV 59
           MK+++ADSI   ++    LE + E+ +  +  ++ +E +D IKD D +VV  R  V+ E 
Sbjct: 1   MKIVVADSIFLTDEYRKRLEALGELEIYDSVPVSLDEFIDRIKDADIVVV-GRYGVSAEA 59

Query: 60  IEAAPRLKIIARAGVGVDNVDVKAATDRGIMVINAPESTSITVAEHSIGLMLALARKIAI 119
           + +APRLK+I+    G DNVD++ ATD G++V N P     +VAE    L L L R++ +
Sbjct: 60  LRSAPRLKMISLWQTGFDNVDLEEATDHGVIVSNVPSYAFESVAEFVFALTLNLLRRVHL 119

Query: 120 ADRSVKEGKWEKNRFMGIELNGKTLGIIGMGRIGSQVVVRTKAFGMDIMVYDPYISKEAA 179
           AD +++EG ++   ++G +L  KT+G++G G IG +V+     F M+++    + S E A
Sbjct: 120 ADMNLREGLFDWKYYVGNQLMSKTIGVLGTGEIGKRVIQIAHGFNMNVLSVTAHPSPERA 179

Query: 180 EEMGVTVTDLETLLRESDIVTIHVPLTPETRHLISEDEFKLMKDTAFIVNCARGGIIDED 239
           + +GV   DL+TLL ESDIVT+HVPLTPET H+I   E   MK TA ++N ARG +++E 
Sbjct: 180 KALGVKFVDLDTLLSESDIVTLHVPLTPETEHMIGARELAKMKPTAILINTARGKVVEEA 239

Query: 240 ALYRALKDGEIAGAALDVFEEEP-PEGSPLLELENVVLTPHIGASTSEAQRDAAIIVANE 298
           AL  ALK+ +IAGA LDVFE EP    SPLLE+ NVVLTPHI A  SE   D    ++ E
Sbjct: 240 ALMEALKEKKIAGAGLDVFEREPLSMDSPLLEMHNVVLTPHI-AFLSEESLDECTYISIE 298

Query: 299 IKTVFQGGAPRNVLNMPVM 317
              +F  G P+NV+N  V+
Sbjct: 299 NVEMFAKGKPQNVVNPSVL 317


Lambda     K      H
   0.316    0.135    0.366 

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: 393
Number of extensions: 19
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: 319
Length adjustment: 31
Effective length of query: 494
Effective length of database: 288
Effective search space:   142272
Effective search space used:   142272
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 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

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