GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ac3H11_1694 in Magnetospirillum magneticum AMB-1

Align ABC transporter ATP-binding protein (characterized, see rationale)
to candidate WP_011384209.1 AMB_RS09130 high-affinity branched-chain amino acid ABC transporter permease LivM

Query= uniprot:A0A165KER0
         (358 letters)



>NCBI__GCF_000009985.1:WP_011384209.1
          Length = 415

 Score =  248 bits (632), Expect = 3e-70
 Identities = 154/353 (43%), Positives = 210/353 (59%), Gaps = 46/353 (13%)

Query: 8   WIIGAVALLVLPLILQSFGNAWVRIADLALLYVLLALGLNIVVGYAGLLDLGYVAFYAVG 67
           W + A AL +LP +  S G   V  A L L+YV+L  GLNIVVG AGLLDLG+VAFYAVG
Sbjct: 89  WAMVAFAL-ILPFLPFS-GRNLVDKATLVLIYVMLGWGLNIVVGLAGLLDLGFVAFYAVG 146

Query: 68  AYLFALMASPHLADNFAAFAAMFPNGLHTSLWIVIPVAALLAAFFGAMLGAPTLKLRGDY 127
           AY +AL++                 GL  S W+ +P+A LLAA FG +LG P L+LRGDY
Sbjct: 147 AYSYALLSQTF--------------GL--SFWVCLPLAGLLAAAFGMVLGFPVLRLRGDY 190

Query: 128 LAIVTLGFGEIIRIFLNNLDHPVNLTNGPKGLGQIDSVKVFGLDL------GKRL--EVF 179
           +AIVT+G GEI+R+ L N     ++T GP G+  I+   +FGL        G +   E F
Sbjct: 191 IAIVTMGLGEIVRVVLQNWQ---DVTGGPNGISGIERPSLFGLSFKMVPPEGSQTFAEFF 247

Query: 180 GFDINS---VTLYYYLFLVLVVVSVIICYRLQDSRIGRAWMAIREDEIAAKAMGINTRNM 236
           G D ++   V   Y+L L L +++ +I  R++   +GRAW A+REDEIA +++GIN   +
Sbjct: 248 GLDYSADHRVIFLYFLILALALLTNVITLRIRRLPVGRAWEALREDEIACRSLGINPTLV 307

Query: 237 KLLAFGMGASFGGVSGAMFGAFQGFVSPESFSLMESVMIVAMVVLGGIGHIPGVILGAVL 296
           KL AF  GA F G +G+ F   QGF+SPESF+ +ES +I+A+VVLGG+G   G++L A+L
Sbjct: 308 KLSAFATGAMFAGFAGSFFATRQGFISPESFTFIESAVILAIVVLGGMGSQIGIVLAALL 367

Query: 297 LSALPEVLRYVAGPLQAMTDGRLDSAILRQLLIALAMIIIMLLRPRGLWPSPE 349
           L  LPE  R              +    R L    AM++IML +P GL  + E
Sbjct: 368 LVGLPEWFR--------------ELQQFRMLAFGGAMVLIMLWKPAGLLSTRE 406


Lambda     K      H
   0.328    0.144    0.430 

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: 435
Number of extensions: 19
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: 358
Length of database: 415
Length adjustment: 30
Effective length of query: 328
Effective length of database: 385
Effective search space:   126280
Effective search space used:   126280
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 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