GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dsdA in Echinicola vietnamensis KMM 6221, DSM 17526

Align D-Serine ammonia-lyase (EC 4.3.1.18) (characterized)
to candidate Echvi_1189 Echvi_1189 Threonine dehydratase

Query= BRENDA::Q54HH2
         (324 letters)



>FitnessBrowser__Cola:Echvi_1189
          Length = 319

 Score =  288 bits (737), Expect = 1e-82
 Identities = 154/311 (49%), Positives = 207/311 (66%), Gaps = 4/311 (1%)

Query: 9   LKDIKEAHKRIEKYIHKTPVLTNSTINELAGKELYFKCENLQKTGSFKMRGACNAIFSLD 68
           L DIK+A++RI  YIH TP+LT   IN++A  +LYFKCEN QK G+FK RGA NAI  L 
Sbjct: 10  LIDIKQAYQRIMAYIHHTPILTCEAINKMADCQLYFKCENFQKVGAFKARGATNAILKLP 69

Query: 69  EEELSKGVVTHSSGNHGQALSYASKVRCVKCYVVVPEDAPSVKLNAICGYGATVTKCKAT 128
                 GV THSSGNH  AL+ A+K    K Y+V+P  A ++K  A+  YG  + +C+  
Sbjct: 70  PGLKKNGVATHSSGNHAAALARAAKETGTKAYIVMPSTAAAIKKAAVRTYGGEIIECEPN 129

Query: 129 LEARESNTKQLIEQHSCKLIHPFDNLQVIAGQGTASLELMEQVENLDAIITPVGGGGLLS 188
           L+ARE+  ++++E+     I P+D + VI GQ T +LE+ ++    DAIITPVGGGGLL+
Sbjct: 130 LKARETTLEKVVEETGAAFIPPYDYMDVIEGQATCALEMWDEGIPFDAIITPVGGGGLLA 189

Query: 189 GTCITAKSLNPNIKVFAAEPLGADDTYRSLLSGEIQKHTPGKPNTIADGLLTTVGSLTFP 248
           GT +T   L+    V+ AEP GADD YRSL + +I       PNTIADGLLT++G   F 
Sbjct: 190 GTALTTHYLSRKTPVYGAEPKGADDAYRSLKANKIIPME--NPNTIADGLLTSLGKRNFT 247

Query: 249 IIKENCDGVILVTEDEIKYAMKLVWERMKIIIEPSSATTLAAILKQEFKDKKDIKKVGII 308
           II +N   ++ V++D+I  AM+LV+ERMK++IEPSSA  LAAIL    K     K+VGI+
Sbjct: 248 IISKNVADILTVSDDQIIAAMRLVFERMKLVIEPSSAVPLAAILAN--KPLFQNKRVGIV 305

Query: 309 ISGGNVDLSSI 319
           ISGGNVD+S +
Sbjct: 306 ISGGNVDVSKL 316


Lambda     K      H
   0.315    0.132    0.374 

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: 291
Number of extensions: 10
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: 324
Length of database: 319
Length adjustment: 28
Effective length of query: 296
Effective length of database: 291
Effective search space:    86136
Effective search space used:    86136
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 (21.5 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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