GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Nitratiruptor tergarcus DSM 16512

Align branched-chain-amino-acid transaminase (EC 2.6.1.42); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate WP_084274637.1 B8779_RS00495 branched-chain amino acid transaminase

Query= BRENDA::P54691
         (305 letters)



>NCBI__GCF_900176045.1:WP_084274637.1
          Length = 304

 Score =  172 bits (435), Expect = 1e-47
 Identities = 101/296 (34%), Positives = 172/296 (58%), Gaps = 14/296 (4%)

Query: 9   YFEDKFVPFEDAKISVATHALHYGTAAFGGLRGIPDPEDPGTILLFRLDRHGDRLSKSAK 68
           +   +FVP++DAK+ V TH LHYG   F G R     +    + +FRL  H  RL  SAK
Sbjct: 8   WMNGEFVPWDDAKVHVLTHTLHYGNGVFEGTRAYKTAKG---LAIFRLRDHTKRLLNSAK 64

Query: 69  FLHYDI--SAEKIKEVIVDFVKKNQPDKSFYIRPLVYSSGLGIAPRLH-NLEKDFLVYGL 125
                +  + E+++   ++ +++N  D + YIRPL+Y  G G+    H N   +  +   
Sbjct: 65  ITAIKVPYTLEELENAQIELLRQNSFDGNVYIRPLIYL-GYGVMGLYHVNAPVEVAIAAW 123

Query: 126 EMGDYLAADG----VSCRISSWYRQEDRSFPLRGKISAAYITSALAKTEAVESGFDEAIL 181
           + G YL  +G    +  ++SS+ R   +S   + K  A Y+ S +AK EA+ +G++EA+L
Sbjct: 124 KWGAYLGDEGLEKGIRVKVSSFARNSVKSTMGKAKAVANYLNSQMAKYEAIIAGYEEALL 183

Query: 182 MNSQGKVCEATGMNVFMVRNGQIVTPGNEQDILEGITRDSILTIAADLGIPTCQRPIDKS 241
           ++ +G V E +G  +F+VR+G +++P N+   LE IT+D+IL IA + GIP  +R + + 
Sbjct: 184 LDEEGFVAEGSGECLFIVRDGVLISPPNDNS-LESITQDTILKIAHEKGIPVERRRVTRD 242

Query: 242 ELMIADEVFLSGTAAKITPVKRIENFTLG-GDR-PITEKLRSVLTAVTENREPKYQ 295
           E+ IADE F +GTAA++TP++ ++   +G G R  +T++L++    +   R P Y+
Sbjct: 243 EVYIADEAFFTGTAAEVTPIREVDGRIIGSGSRGEMTKELQTAYFDIVYGRNPAYE 298


Lambda     K      H
   0.320    0.138    0.406 

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: 221
Number of extensions: 11
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: 305
Length of database: 304
Length adjustment: 27
Effective length of query: 278
Effective length of database: 277
Effective search space:    77006
Effective search space used:    77006
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: 48 (23.1 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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