GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Sphingomonas wittichii RW1

Align Homoserine O-succinyltransferase; HST; EC 2.3.1.46; Homoserine transsuccinylase; HTS (uncharacterized)
to candidate WP_012049205.1 SWIT_RS15195 homoserine O-acetyltransferase

Query= curated2:A0LCI7
         (394 letters)



>NCBI__GCF_000016765.1:WP_012049205.1
          Length = 378

 Score =  379 bits (972), Expect = e-109
 Identities = 199/362 (54%), Positives = 247/362 (68%), Gaps = 15/362 (4%)

Query: 26  PLQLDGGTLLHSVDVSYETYGTLNQERSNAVLICHALSGNAHAAGYHSKDDKRPGWWDHY 85
           PL+LDGG  L  V+++YETYG+L+ +  NAVLICHAL+G+ H A  H    K PGWW   
Sbjct: 21  PLRLDGGARLAPVEIAYETYGSLDADGGNAVLICHALTGDQHVASTHPITGK-PGWWTRM 79

Query: 86  IGPGKPFDTNRYFVIASNNLGGCDGTTGPSSIDPATGMPYGLNFPMITIGDIVRVQHALV 145
           +G GKP D  R+F+I +N LG C G++GP +IDPATG PY + FP+ITI D+VR Q  L+
Sbjct: 80  VGAGKPIDPARHFIICANVLGSCLGSSGPGTIDPATGAPYAMRFPVITIRDMVRAQAILL 139

Query: 146 RQLGIERLMAVVGGSMGGMQALQWALDYPHMVPASVIIAAAPRLTAQNIAFNAVARQAIM 205
             LG+  L A VGGSMGGMQ LQWA  YP  + ++V IA+  R +AQNIAF+ V RQAIM
Sbjct: 140 DHLGVGTLAAAVGGSMGGMQVLQWAATYPDRLRSAVAIASTARHSAQNIAFHEVGRQAIM 199

Query: 206 ADPHFNGGDYYTLPGDPTTKARPESGLALARMMAHITYLSEQGLHERFGRRLQDRDALSY 265
           ADP + GGDYY   GDP     P +GLA+ARM AHITYLSE GL E+FGRRLQ RDA S+
Sbjct: 200 ADPKWAGGDYYA-AGDP-----PAAGLAVARMAAHITYLSEAGLTEKFGRRLQARDAKSF 253

Query: 266 GFETDFAVESYLSYQGSSFVKRFDANSYLYITKAMDYFDPFPDAETTVQRLTGV-----E 320
           GF+ DF +ESYL +QG SFV RFDANSYLYIT+AMDYFD    AE     L G       
Sbjct: 254 GFDADFQIESYLRHQGISFVDRFDANSYLYITRAMDYFDL---AEEHGGLLAGAFQGAKR 310

Query: 321 SHFLVMSFDTDWRFDTSRSKELVRILHRSLKDCTFQEFSSPAGHDAFLLPHPSYEKSLGS 380
           + F ++SFDTDW + T+ S+ +V  L+ +    +F E SSP GHDAFLL  P   + +  
Sbjct: 311 TRFCLVSFDTDWLYPTAESRAIVHALNAAGAPVSFVELSSPFGHDAFLLDVPELNRVVDG 370

Query: 381 FL 382
           FL
Sbjct: 371 FL 372


Lambda     K      H
   0.320    0.136    0.417 

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: 515
Number of extensions: 22
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: 394
Length of database: 378
Length adjustment: 30
Effective length of query: 364
Effective length of database: 348
Effective search space:   126672
Effective search space used:   126672
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 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