GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ARO8 in Dinoroseobacter shibae DFL-12

Align Aspartate aminotransferase; AAT; AspAT; EC 2.6.1.1 (characterized)
to candidate 3607759 Dshi_1168 aminotransferase class I and II (RefSeq)

Query= SwissProt::Q82DR2
         (408 letters)



>FitnessBrowser__Dino:3607759
          Length = 391

 Score =  174 bits (441), Expect = 4e-48
 Identities = 123/380 (32%), Positives = 185/380 (48%), Gaps = 22/380 (5%)

Query: 31  AKALKAAGRPVIGFGAGEPDFPTPDYIVQAAIEACSNPKYHRYTPAGGLPELKAAIAAKT 90
           A+  +AAGR +I    G+P    P    + A+ A  +     YT A GLPEL+ AIA   
Sbjct: 21  ARRAEAAGRHIIHMEVGQPGTAAP-LPARRAVAAQLDQDAMGYTVALGLPELRRAIAGLY 79

Query: 91  LRDSGYEVDASQVLVTNGGKQAIYEAFAAILDPGDEVIVPAPYWTTYPESIRLAGGVPVD 150
            R  G ++D ++V+VT+G   A   AF    D G  V V  P + +Y + ++     PV 
Sbjct: 80  ARWYGVDLDPARVVVTSGSSAAFLLAFTTYFDAGARVGVAEPGYPSYRQILKALSLAPVG 139

Query: 151 VVADETTGYRVSVEQLEAARTENTKVLLFVSPSNPTGAVYTREQIEEIGRWAAEKGLWVL 210
           +     TG+R++ E L  A        +  SP+NPTG +  R+ +  +     ++    +
Sbjct: 140 LPTQPETGHRMTAEALAQADIAGA---IIASPNNPTGTMLDRDGLGALIAACRDRDRVFI 196

Query: 211 TDEIYEHLVYGDAEFHSLPVVVPELADKCIVVNGVAKTYAMTGWRVGWVIGPKDVIKAAT 270
           +DEIY  L YGD    +L     E++D   V+N  +K ++MTGWR+GW++ P+  ++   
Sbjct: 197 SDEIYHGLHYGDRAVSAL-----EISDDVCVINSFSKYFSMTGWRIGWLVVPEAQVRVVE 251

Query: 271 NLQSHATSNVSNVAQVAALAAVSGDLTAVAEM-REAFDRRRKTIVRMLNEIGGVLCPEPE 329
            L  +      +VAQ+AAL A+        E  R  +   R+ ++  L   G      P+
Sbjct: 252 RLAQNMFICAPHVAQIAALGALGDAARPELEANRAVYAANRQLVIDGLRAAGLDAFAPPD 311

Query: 330 GAFYAYPSVKALLGKEIRGKRPQDTVELAALILEEAEVAVVPGEAFGT---PGYLRLSYA 386
           GAFY Y    AL           D+  LAA ILE+A VAV PG  F      G LRLSYA
Sbjct: 312 GAFYVYVDTGAL---------SSDSRTLAADILEKAGVAVTPGLDFDPVRGHGTLRLSYA 362

Query: 387 LGDEDLVEGVSRIQKLLSEA 406
              ED+ EG++R+    + A
Sbjct: 363 RATEDIAEGMTRLTNYFAAA 382


Lambda     K      H
   0.315    0.132    0.381 

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: 360
Number of extensions: 13
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: 408
Length of database: 391
Length adjustment: 31
Effective length of query: 377
Effective length of database: 360
Effective search space:   135720
Effective search space used:   135720
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 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