GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Chlorobium phaeobacteroides BS1

Align Putative (R)-citramalate synthase CimA; EC 2.3.3.21 (uncharacterized)
to candidate WP_012475142.1 CPHAMN1_RS08710 homocitrate synthase

Query= curated2:O29305
         (489 letters)



>NCBI__GCF_000020545.1:WP_012475142.1
          Length = 383

 Score =  228 bits (582), Expect = 2e-64
 Identities = 132/368 (35%), Positives = 209/368 (56%), Gaps = 4/368 (1%)

Query: 5   ILDTTLRDGEQTPGVSLSVEQKVMIAEALDNLGVDIIEAGTAIASEGDFQAIKEISQRGL 64
           I+DTTLRDGEQ PGV  S E+K  IA  + ++G D +E G    S  + + I+EI    L
Sbjct: 9   IIDTTLRDGEQAPGVVFSPEEKKDIAAMIADIGADELEIGYPAISVDEQRVIREIVAMKL 68

Query: 65  NAEICSFARIKREDIDAAADAGAESIFMVAPSSDIHINAKFPGKDRDYVIEKSVEAIEYA 124
              +  ++R KR DI+ A+    E I +  P S+++++    GKD  +V E+    I  A
Sbjct: 69  PKRLTCWSRAKRSDIECASRCETEGIHISFPISNLYLDLM--GKDYLWVREQLEILIPEA 126

Query: 125 KERGLIVEFGAEDASRADLDFVIQLFKRAEEAKADRITFADTVGVLSPEKMEEIVRKIKA 184
           K+    V  GA+DA+R D+  +    + A    ADR+  ADTVG+ +P  +   + ++K+
Sbjct: 127 KKHFSFVSAGAQDATRTDVTTLEAFARDASLCGADRVRIADTVGIATPLTLMRHIEQLKS 186

Query: 185 KVKLPLAIHCHDDFGLATANTIFGIKAGAEEFHGTINGLGERAGNAAIEEVVIALEYLYG 244
            V +PL  H H+D G+ATAN    I+AG +    ++NGLGERAGNAA+EE+ +AL+    
Sbjct: 187 SVTIPLEFHAHNDLGMATANAFSAIEAGCDAVSVSVNGLGERAGNAALEELSLALKLSGR 246

Query: 245 IKTKIKKERLYNTSKLVEKLSRVVVPPNKPIVGDNAFTHESGIHTSALFRDAKSYEPISP 304
            +  IK +RL+   + V K S  ++   KP+ G   F HESGIH +AL +D  SY+P  P
Sbjct: 247 YRNSIKTDRLHRLCEKVAKASNRIIQDQKPVTGSAVFQHESGIHCNALLKDPLSYQPFLP 306

Query: 305 EVVGRKRV-IVLGKHAGRASVEAIMNELGYKATPEQMKEILARIKEIGDKGKR-VTDADV 362
             +G++   +V+GKH+G AS++  M   G     E+  ++L  ++   ++ K  ++ A++
Sbjct: 307 GDIGKEAYELVIGKHSGSASIQHAMEANGISIDREEAGKMLLSVRLAANRKKSGLSSAEL 366

Query: 363 RTIIETVL 370
             I +  L
Sbjct: 367 MNIYKECL 374


Lambda     K      H
   0.317    0.135    0.364 

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: 383
Number of extensions: 12
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: 489
Length of database: 383
Length adjustment: 32
Effective length of query: 457
Effective length of database: 351
Effective search space:   160407
Effective search space used:   160407
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: 51 (24.3 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