GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ARO8 in Desulfobacter vibrioformis DSM 8776

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate WP_035242342.1 Q366_RS18995 aminotransferase

Query= BRENDA::Q8YTF2
         (403 letters)



>NCBI__GCF_000745975.1:WP_035242342.1
          Length = 399

 Score =  347 bits (891), Expect = e-100
 Identities = 166/384 (43%), Positives = 243/384 (63%), Gaps = 3/384 (0%)

Query: 9   ADRIQQLPPYVFARLDELKAKAREQGIDLIDLGMGNPDGATPQPVVDAAIQALQDPKNHG 68
           A R+  LPPY+F  ++++K + R +G D+IDLGMGNP   TP  V++  ++  +DPK+H 
Sbjct: 10  ASRMDYLPPYLFGMINKMKMEKRRKGDDVIDLGMGNPMDPTPDAVIEKLVEVAKDPKSHR 69

Query: 69  YPPFEGTASFRRAITNWYNRRYGVVLDPDSEALPLLGSKEGLSHLAIAYVNPGDVVLVPS 128
           YP   G    +R I  +Y R Y + LD D E    +GSKEG+SHL +A + PGD VLVP+
Sbjct: 70  YPESSGLPHLKREIAKYYGRHYNIGLDADKETYFTIGSKEGISHLCLAIMGPGDCVLVPA 129

Query: 129 PAYPAHFRGPVIAGGTVHSLILKPENDWLIDLTAIPEEVARKAKILYFNYPSNPTGATAP 188
           PA+P H    VIAG  V  + L+PE  +L  +  + E      K+L  NYP NPTG    
Sbjct: 130 PAFPIHIYAAVIAGANVMRIPLEPEKGFLDRIIKVCEACYPSPKVLMLNYPHNPTGVVTD 189

Query: 189 REFFEEIVAFARKYEILLVHDLCYAELAFDGYQPTSLLEIPGAKDIGVEFHTLSKTYNMA 248
           + F++EIV  A++++ ++++D  YA++ +DGY   S LEI GAKD+GVEF + SK+YNMA
Sbjct: 190 KNFYKEIVKLAKRFKFMVINDFAYAKITYDGYVAPSFLEIEGAKDVGVEFGSFSKSYNMA 249

Query: 249 GWRVGFVVGNRHVIQGLRTLKTNLDYGIFAALQTAAETALQLPDIYLHEVQQRYRTRRDF 308
           GWR+G+ VGN  +++ L  +K   DYGIF+A+Q A   AL+  D  + E+ + Y  RRD 
Sbjct: 250 GWRIGYCVGNEKIVEALGKIKGYFDYGIFSAIQVAGIIALRDCDDTIPELVKIYENRRDV 309

Query: 309 LIQGLGELGWDVPKTKATMYLWVKCPV---GMGSTDFALNLLQQTGVVVTPGNAFGVAGE 365
           L  GL  +GWD+ K KA M++W K P     MGS +FA+ L+    V V PG  F   GE
Sbjct: 310 LCSGLERIGWDIQKPKAGMFVWAKIPEPFNKMGSMEFAIQLMNNGNVAVAPGAGFSEEGE 369

Query: 366 GYVRISLIADCDRLGEALDRIKQA 389
           GY+R++L+ + +RL +A+ ++K+A
Sbjct: 370 GYLRLALVENEERLRQAVRQMKKA 393


Lambda     K      H
   0.321    0.140    0.427 

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: 459
Number of extensions: 17
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: 403
Length of database: 399
Length adjustment: 31
Effective length of query: 372
Effective length of database: 368
Effective search space:   136896
Effective search space used:   136896
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 Sep 24 2021. The underlying query database was built on Sep 17 2021.

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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