GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metB in Mesorhizobium ciceri WSM1271

Align cystathionine gamma-synthase (EC 2.5.1.48) (characterized)
to candidate YP_004143819.1 Mesci_4660 cystathionine beta-lyase

Query= BRENDA::H7C6A2
         (386 letters)



>NCBI__GCF_000185905.1:YP_004143819.1
          Length = 393

 Score =  197 bits (500), Expect = 6e-55
 Identities = 125/382 (32%), Positives = 197/382 (51%), Gaps = 14/382 (3%)

Query: 9   GFSTASIHAGYEPDDYYGSINTPI-YASTTFAQNAPNELRKGYEYT--RVGNPTIVALEQ 65
           G +T   H+G  P DY+G +N P+ +AST   ++A +   +  +YT    G PT  AL  
Sbjct: 13  GINTRLAHSGNNPHDYFGFVNPPVVHASTVLFRDAASMAARTQKYTYGTRGTPTTDALAH 72

Query: 66  TVAALEGAKYGRAFSSGMAATDILFRIILKPGDHIVLGNDAYGGTYRLIDTVFTAWGVEY 125
            + ALEG+       SG+AA  +     +  GDH+++ +  Y  T    DT+    GVE 
Sbjct: 73  AIDALEGSAGTILVPSGLAAVTVPLLAFVSAGDHLLIVDTVYHPTRNFADTMLKRLGVEV 132

Query: 126 TVVDTSVVEEVKAAIKDNTKLIWVETPTNPALGITDIEAVAKLTEGTNAKLVVDNTFASP 185
                 V   + A IK NTK+++ E+P +    + DI A+AK      A +++DNT+A+P
Sbjct: 133 EYYAPHVGAGIAALIKPNTKVVFTESPASNTFEVQDIPAIAKAAHAAGAIVMMDNTWATP 192

Query: 186 YLQQPLKLGAHAVLHSTTKYIGGHSDVVGGLVVTNDQ---EMDEELLFMQGGIGPIPSVF 242
              +PL  G    +H+ TKY  GHSDV+ G V  N+     + E    +    GP     
Sbjct: 193 LYFRPLDHGVDISIHAATKYPAGHSDVLLGTVSANESCWTHLYESFCTLGCCAGP----D 248

Query: 243 DAYLTARGLKTLAVRMDRHCDNAEKIAEFLDSRPEVSTVLYPGLKNHPGHEVAAKQMKRF 302
           D Y   RGL+++ VR++ H  +   IA +L+ +  V+ VL+P L +HP HE+  +     
Sbjct: 249 DVYQVLRGLRSMGVRLEHHQRSTLAIASWLEGQKGVARVLHPALPSHPDHELWKRDFSGS 308

Query: 303 GGMISVRFA-GGEEAAKKFCTSTKLICLAESLGGVESLLEHPATMTHQSAAGSQLEVPRD 361
            G+ S+  A GG++    F  + ++  L  S GG ESL   P  +  +  A +  E P  
Sbjct: 309 SGIFSIVLAGGGQKQQHAFLDALQIFGLGYSWGGYESLAV-PVWLGDRVVAKAPYEGP-- 365

Query: 362 LVRISIGIEDIEDLLADVEQAL 383
           L+R+ IG+ED++DL AD+ + L
Sbjct: 366 LIRLQIGLEDVDDLKADISRGL 387


Lambda     K      H
   0.316    0.134    0.385 

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: 432
Number of extensions: 29
Number of successful extensions: 5
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: 386
Length of database: 393
Length adjustment: 30
Effective length of query: 356
Effective length of database: 363
Effective search space:   129228
Effective search space used:   129228
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.

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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