GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Methylobacterium sp. 4-46

Align Solute-binding (Aliphatic amino acid) component of ABC transporter (characterized, see rationale)
to candidate WP_012335132.1 M446_RS26235 branched-chain amino acid ABC transporter substrate-binding protein

Query= uniprot:Q1MDE9
         (367 letters)



>NCBI__GCF_000019365.1:WP_012335132.1
          Length = 372

 Score =  337 bits (865), Expect = 2e-97
 Identities = 171/350 (48%), Positives = 230/350 (65%), Gaps = 1/350 (0%)

Query: 10  LVASLAFAPLAHADITIGLIAPLTGPVAAYGDQVKNGAQTAVDEINKKGGILGEKVVLEL 69
           + A LAFA  A A I I +  P+TG  AA+G Q+KNGA  AV++INK GGILG+K+VL  
Sbjct: 8   VAAGLAFAGSAQAQIKIAVAGPITGANAAFGAQLKNGAVQAVEDINKAGGILGQKIVLVD 67

Query: 70  ADDAGEPKQGVSAANKVVGDGIRFVVGPVTSGVAIPVSDVLAENGVLMVTPTATAPDLTK 129
            DDA +PKQGVS ANK   +G++ VVG   SGV+IP S+V AE+G++ +TP +T P  T 
Sbjct: 68  GDDASDPKQGVSVANKFAAEGVKAVVGHFNSGVSIPASEVYAESGIVQITPASTNPKFTD 127

Query: 130 RGLTNVLRTCGRDDQQAEVAAKYVLKNFKDKRVAIVNDKGAYGKGLADAFKATLNAGGIT 189
           R L N  RTCGRDDQQ  VA  Y+  +FK K VA V+DK  YG+GLAD     L A G  
Sbjct: 128 RKLWNTFRTCGRDDQQGAVAGAYLASHFKGKNVAFVHDKTPYGRGLADETLKALKAKGGK 187

Query: 190 EVVNDAITPGDKDFSALTTRIKSEKVDVVYFGGYHPEGGLLARQLHDLAANATIIGGDGL 249
           +V+ + I PG+KD+SAL +++K  K DVVYFGG HPE GL+ RQ+HD   N  ++ GDG+
Sbjct: 188 DVLFEGINPGEKDYSALVSKLKQAKTDVVYFGGLHPEAGLIVRQMHDQGLNVPLMSGDGI 247

Query: 250 SNTEFWAIGTDAAGGTIFTNASDATKSPDSKAAADALAAKNIPAEAFTLNAYAAVEVLKA 309
           ++ EF  I    A GT+ T + DA K+P++K    A  AKNI  EA+TL +YAA ++LKA
Sbjct: 248 TDKEFAQIAGPGADGTLMTFSPDARKNPNAKDVVAAFKAKNIDPEAYTLYSYAAFQILKA 307

Query: 310 GIEKAGSAEDAEAVATALKDGKEIPTAIGKVTYGETGDLTSQSFSLYKWE 359
            +E+A S  D++ VA  +  GK   T IG + Y + GD+T   + +Y W+
Sbjct: 308 AMEEAKST-DSKKVAEIMHSGKPFKTVIGDIAYDKKGDITRPDYVMYVWK 356


Lambda     K      H
   0.312    0.131    0.362 

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: 406
Number of extensions: 13
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: 367
Length of database: 372
Length adjustment: 30
Effective length of query: 337
Effective length of database: 342
Effective search space:   115254
Effective search space used:   115254
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 49 (23.5 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