GapMind for catabolism of small carbon sources

 

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

Align Transmembrane component of a broad range amino acid ABC transporter (characterized, see rationale)
to candidate WP_011384209.1 AMB_RS09130 high-affinity branched-chain amino acid ABC transporter permease LivM

Query= uniprot:Q1MCU1
         (463 letters)



>NCBI__GCF_000009985.1:WP_011384209.1
          Length = 415

 Score =  385 bits (990), Expect = e-111
 Identities = 201/314 (64%), Positives = 242/314 (77%), Gaps = 17/314 (5%)

Query: 142 ILIYVMLAWGLNIVVGLAGLLDLGYVAFYAVGAYSYALLSSYFGLSFWVLLPLSGIFAAL 201
           +LIYVML WGLNIVVGLAGLLDLG+VAFYAVGAYSYALLS  FGLSFWV LPL+G+ AA 
Sbjct: 115 VLIYVMLGWGLNIVVGLAGLLDLGFVAFYAVGAYSYALLSQTFGLSFWVCLPLAGLLAAA 174

Query: 202 WGVILGFPVLRLRGDYLAIVTLAFGEIIRLVLINWTDVTKGTFGISSIPKATLFGIPFDA 261
           +G++LGFPVLRLRGDY+AIVT+  GEI+R+VL NW DVT G  GIS I + +LFG+ F  
Sbjct: 175 FGMVLGFPVLRLRGDYIAIVTMGLGEIVRVVLQNWQDVTGGPNGISGIERPSLFGLSFKM 234

Query: 262 T----AGGFAKLFHLPISSAYYKIFLFYLILALCMLTAYVTIRLRRMPIGRAWEALREDE 317
                +  FA+ F L  S+ +  IFL++LILAL +LT  +T+R+RR+P+GRAWEALREDE
Sbjct: 235 VPPEGSQTFAEFFGLDYSADHRVIFLYFLILALALLTNVITLRIRRLPVGRAWEALREDE 294

Query: 318 IACRSLGINTVTTKLTAFATGAMFAGFAGSFFAARQGFVSPESFVFLESAVILAIVVLGG 377
           IACRSLGIN    KL+AFATGAMFAGFAGSFFA RQGF+SPESF F+ESAVILAIVVLGG
Sbjct: 295 IACRSLGINPTLVKLSAFATGAMFAGFAGSFFATRQGFISPESFTFIESAVILAIVVLGG 354

Query: 378 MGSLTGIAIAAIVMVGGTELLREMSFLKLIFGPDFTPELYRMLIFGLAMVVVMLFKPRGF 437
           MGS  GI +AA+++VG  E  RE+             + +RML FG AMV++ML+KP G 
Sbjct: 355 MGSQIGIVLAALLLVGLPEWFREL-------------QQFRMLAFGGAMVLIMLWKPAGL 401

Query: 438 VGSREPTAFLRERK 451
           + +REPT  L E K
Sbjct: 402 LSTREPTIRLGEAK 415


Lambda     K      H
   0.330    0.145    0.432 

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: 656
Number of extensions: 41
Number of successful extensions: 3
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: 463
Length of database: 415
Length adjustment: 32
Effective length of query: 431
Effective length of database: 383
Effective search space:   165073
Effective search space used:   165073
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 (21.8 bits)
S2: 51 (24.3 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