GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gly1 in Alkalihalobacterium alkalinitrilicum DSM 22532

Align L-threonine aldolase (EC 4.1.2.5) (characterized)
to candidate WP_078428032.1 BK574_RS06730 low-specificity L-threonine aldolase

Query= BRENDA::Q9X266
         (343 letters)



>NCBI__GCF_002019605.1:WP_078428032.1
          Length = 342

 Score =  365 bits (938), Expect = e-106
 Identities = 185/338 (54%), Positives = 248/338 (73%), Gaps = 1/338 (0%)

Query: 2   IDLRSDTVTKPTEEMRKAMAQAEVGDDVYGEDPTINELERLAAETFGKEAALFVPSGTMG 61
           IDLRSDTVTKPTEEMR+AM  AEVGDDVYGEDPTIN LE LAA+  GKE ALFV SGT G
Sbjct: 4   IDLRSDTVTKPTEEMRQAMLTAEVGDDVYGEDPTINRLEALAAKMLGKEDALFVTSGTQG 63

Query: 62  NQVSIMAHTQRGDEVILEADSHIFWYEVGAMAVLSGVMPHPVPGKNGAMDPDDVRKAIRP 121
           NQV+I+ H + GDE+ILEA++HIF YE GA + L+GV    + G  G MDP  ++KAIR 
Sbjct: 64  NQVAILTHCRPGDELILEAEAHIFLYEGGAASALAGVQTRTISGIKGEMDPLAIKKAIRG 123

Query: 122 RNIHFPRTSLIAIENTHNRSGGRVVPLENIKEICTIAKEHGINVHIDGARIFNASIASGV 181
            +IH+P + LI +ENTHN++GG+VVPL+ +KEI  IA+E  + +H+DGAR+FNA++A+GV
Sbjct: 124 EDIHYPYSGLICLENTHNKAGGKVVPLQTMKEIHEIAREKDVPIHLDGARLFNAAVATGV 183

Query: 182 PVKEYAGYADSVMFCLSKGLCAPVGSVVVGDRDFIERARKARKMLGGGMRQAGVLAAAGI 241
           PV ++  Y D+V  CLSKGL APVGS++ G+  FI+ ARK RK LGGG+RQAGVLAA GI
Sbjct: 184 PVADFTQYVDTVQVCLSKGLSAPVGSILAGNTAFIKEARKWRKRLGGGLRQAGVLAAPGI 243

Query: 242 IALTKMVDRLKEDHENARFLALKLKEI-GYSVNPEDVKTNMVILRTDNLKVNAHGFIEAL 300
           IAL KM++RLKEDH+NA+ LA  L  +    V+ E V+TN+++       ++   F+  L
Sbjct: 244 IALEKMINRLKEDHKNAQLLAELLANVPRLHVDVEGVETNILLCNIKETGLSNEEFLTKL 303

Query: 301 RNSGVLANAVSDTEIRLVTHKDVSRNDIEEALNIFEKL 338
           +++ +LA    D  IR VTH++V+   +E A+   +++
Sbjct: 304 KDASILAGPFDDGIIRFVTHREVTSEMVEAAVQKIKQI 341


Lambda     K      H
   0.319    0.135    0.384 

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: 330
Number of extensions: 9
Number of successful extensions: 2
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: 343
Length of database: 342
Length adjustment: 29
Effective length of query: 314
Effective length of database: 313
Effective search space:    98282
Effective search space used:    98282
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 (21.7 bits)
S2: 49 (23.5 bits)

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