GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Phaeobacter inhibens BS107

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate GFF262 PGA1_c02740 sn-glycerol-3-phosphate import ATP-binding protein UgbC

Query= BRENDA::Q70HW1
         (384 letters)



>FitnessBrowser__Phaeo:GFF262
          Length = 348

 Score =  327 bits (838), Expect = 3e-94
 Identities = 187/366 (51%), Positives = 234/366 (63%), Gaps = 23/366 (6%)

Query: 1   MARVLLEHIYKTYPGQTEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEG 60
           MA+V L  + K YP   E  V   +  I+D EF V VGPSGCGK+T LRMIAGLEDITEG
Sbjct: 1   MAQVTLNSVRKVYPNGVE-AVTSSSFKIEDGEFVVLVGPSGCGKSTLLRMIAGLEDITEG 59

Query: 61  NLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAA 120
            L IGDR VN+V P DRDIAMVFQNYALYPHMTV +N+A+GLK RK P+AEI ++V EAA
Sbjct: 60  TLEIGDRVVNNVDPADRDIAMVFQNYALYPHMTVRKNIAYGLKNRKTPEAEIKQKVAEAA 119

Query: 121 KILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRK 180
           K+L++   LDRKP  LSGGQRQRVA+GRAIVR+P +FL DEPLSNLDAKLR QMR EI+ 
Sbjct: 120 KMLNLEEYLDRKPSQLSGGQRQRVAMGRAIVRDPALFLFDEPLSNLDAKLRNQMRIEIKA 179

Query: 181 LHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPA 240
           L +RL  T IYVTHDQ EAMTM DRI+V+  G I+Q  TP  +Y  P ++FVA F+G+P 
Sbjct: 180 LQRRLGVTSIYVTHDQVEAMTMADRIIVLNGGRIEQIGTPSEIYHNPASVFVASFMGAPP 239

Query: 241 MNFIRGEIVQDGDAFYFRAPSISLRLPEG-RYGVLKASGAIGKPVVLGVRPEDLHDEEVF 299
           MN +   I               + LP+G   G L  S      V LG+RPED+      
Sbjct: 240 MNLLDATIANG-----------QVTLPDGVSMGALDTSAQ--GAVKLGIRPEDVQ----- 281

Query: 300 MTTYPDSVLQMQVEVVEHMGSEVYLHTSIGPNTIVARVNPRHVYHVGSSVKLAIDLNKIH 359
                +  L + VE++E +G+   LH  +G       V        G+  ++++D   I 
Sbjct: 282 --LVAEGGLAIDVELIEELGAHRLLHGKLGGQPFTIHVLKDIPVDPGTH-QISVDPAAIC 338

Query: 360 IFDAET 365
           +FDAE+
Sbjct: 339 LFDAES 344


Lambda     K      H
   0.321    0.138    0.395 

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: 377
Number of extensions: 15
Number of successful extensions: 1
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: 384
Length of database: 348
Length adjustment: 30
Effective length of query: 354
Effective length of database: 318
Effective search space:   112572
Effective search space used:   112572
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: 49 (23.5 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