GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD in Stenotrophomonas chelatiphaga DSM 21508

Align Acetylornithine aminotransferase; ACOAT; EC 2.6.1.11 (uncharacterized)
to candidate WP_057509163.1 ABB28_RS13760 glutamate-1-semialdehyde 2,1-aminomutase

Query= curated2:Q8FTN2
         (402 letters)



>NCBI__GCF_001431535.1:WP_057509163.1
          Length = 426

 Score =  139 bits (349), Expect = 2e-37
 Identities = 116/334 (34%), Positives = 156/334 (46%), Gaps = 25/334 (7%)

Query: 15  PQVLLNTYGTPPVELVTGKGSTVTDADGNVYIDLLAGIAVNALGHAHPAIIEAVTTQLSQ 74
           P     + G  P  +    G+ + D DGN YID +       +GH HPA+ +AV      
Sbjct: 24  PVRAFKSVGGEPFFVERADGAYLHDVDGNRYIDYVGSWGPMIVGHNHPAVRQAVKKAAD- 82

Query: 75  LGHVSNLFATRPVVEVAAELVQRFALDDATIASQTQVFFCNSGAEANEAAFKLAR-LTGR 133
               S L    P    AAE+     L    + S   V   NSG EA  +A +LAR  TGR
Sbjct: 83  ----SGLSFGAPC---AAEVTMAETLT-RLVPSCEMVRMVNSGTEATLSAIRLARGATGR 134

Query: 134 HRILAATNGFHGRTMGSL--ALTGQPDKRIPFAP-LPSGVE----FYPYGDLDYLTTLVE 186
            RI+     +HG     L  A +G     +P +P +P+G+       PY D D  T L E
Sbjct: 135 SRIVKFEGCYHGHGDSFLVKAGSGMLTLGVPTSPGVPAGLSELTLTLPYNDFDAATALFE 194

Query: 187 SDPTDTAAIILEPIQGETGVIPAPEGFLTGVRELCDKHGLLFIVDEVQTGIGRTGDFFAH 246
           +     A +I+EP+ G    IP  EG+L  +R LC + G + I DEV TG  R     A 
Sbjct: 195 AQGEQIAGLIIEPVVGNANCIPPREGYLQHLRALCTRFGTVLIFDEVMTGF-RVALGGAQ 253

Query: 247 QHEGVTPDVVTMAKGLGGGLPIGACLATGEAAKLF---GPGKHGTTFGGNPVSAAAARAV 303
            H GVTPD+ T  K +GGG+P+GA     E  +     GP     T  GNPV+ AA  A+
Sbjct: 254 AHYGVTPDLTTFGKIIGGGMPVGAYGGKRELMQQISPAGPIYQAGTLSGNPVAMAAGLAM 313

Query: 304 LSVIDEE-FCADV-ARKGELFA--EQLRGVAGVA 333
           L ++ +  F A + AR   L A  EQ    AGV+
Sbjct: 314 LELVQQPGFHAQLSARAARLCAGLEQAAAEAGVS 347


Lambda     K      H
   0.319    0.137    0.398 

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: 402
Number of extensions: 24
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: 402
Length of database: 426
Length adjustment: 31
Effective length of query: 371
Effective length of database: 395
Effective search space:   146545
Effective search space used:   146545
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: 50 (23.9 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