GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metC in Dinoroseobacter shibae DFL-12

Align cystathionine gamma-lyase (EC 4.4.1.1) (characterized)
to candidate 3609021 Dshi_2410 O-succinylhomoserine sulfhydrylase (RefSeq)

Query= BRENDA::Q5H4T8
         (397 letters)



>FitnessBrowser__Dino:3609021
          Length = 392

 Score =  266 bits (680), Expect = 8e-76
 Identities = 151/341 (44%), Positives = 222/341 (65%), Gaps = 7/341 (2%)

Query: 56  FEYSRTHNPTRFAYERCVAALEGGTRAFAFASGMAATSTVM-ELLDAGSHVVAMDDLYGG 114
           F Y+R  NPT   +E  +AA+EG   AFA ASGMAA +  +  +L AG HVV+   L+G 
Sbjct: 53  FIYARYGNPTVRMFEDRIAAVEGTEDAFATASGMAAVNGALASMLRAGDHVVSARALFGS 112

Query: 115 TFRLFERVRRRTAGLDFSFVDLTDPAAFKAAIRADTKMVWIETPTNPMLKLVDIAAIAVI 174
              + E V  R  G++ +FVD TD AA++AAIR DTK V+ ET +NP L+++DI A+A +
Sbjct: 113 CLYILEEVLTRY-GVEVTFVDGTDLAAWRAAIRPDTKAVFFETISNPTLEVIDIEAVAKL 171

Query: 175 ARKHGLLTVVDNTFASPMLQRPLSLGADLVVHSATKYLNGHSDMVGGIAVVGDNAELAEQ 234
           A   G L +VDN FA+P+  R    GAD++V+SATK+++G    +GG  V+    +   +
Sbjct: 172 AHAVGALVIVDNVFATPIFSRAKDQGADVIVYSATKHIDGQGRCLGG--VICGTRDFVRK 229

Query: 235 MA--FLQNSIGGVQGPFDSFLALRGLKTLPLRMRAHCENALALAQWLETHPAIEKVIYPG 292
           +A  +L+++ GG   PF++++ L+ ++TL LR+RA  E A ALA+ LE H A+EKVI+P 
Sbjct: 230 VAEPYLKHT-GGSLSPFNAWVMLKSMETLDLRVRAQAETAQALAETLEGHAALEKVIFPH 288

Query: 293 LASHPQHVLAKRQMSGFGGIVSIVLKGGFDAAKRFCEKTELFTLAESLGGVESLVNHPAV 352
           L SHPQ+ LA+ QM+  G ++++ +KGG   A RF    E+ T++ +LG  +S+  HPA 
Sbjct: 289 LPSHPQYDLARAQMAAGGTVLALDIKGGKAGAFRFLNALEIVTISNNLGDAKSIATHPAT 348

Query: 353 MTHASIPVARREQLGISDALVRLSVGIEDLGDLRGDLERAL 393
            TH  +   +R  LGI+D L+RLSVG+ED GDL  DL+ AL
Sbjct: 349 TTHQRLTPEQRAGLGITDGLIRLSVGLEDAGDLLRDLQTAL 389


Lambda     K      H
   0.320    0.134    0.391 

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: 394
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: 397
Length of database: 392
Length adjustment: 31
Effective length of query: 366
Effective length of database: 361
Effective search space:   132126
Effective search space used:   132126
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 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