Align MFS transporter (characterized, see rationale)
to candidate CCNA_01576 CCNA_01576 major facilitator superfamily transporter
Query= uniprot:A0A166QG26 (467 letters) >FitnessBrowser__Caulo:CCNA_01576 Length = 431 Score = 378 bits (970), Expect = e-109 Identities = 193/455 (42%), Positives = 269/455 (59%), Gaps = 47/455 (10%) Query: 14 QAVGNYRWTICALLFFATTVNYLDRQVLSLLAPDLSTQFGWSNSDYANIASVFQFVYAIS 73 + +G YRW I LLF A +NY+DRQ + L DLS +FGWS DYAN+ FQ YA++ Sbjct: 18 EKIGRYRWIIVTLLFLAMVINYVDRQTIGFLKHDLSVEFGWSEHDYANLVFYFQLSYAVA 77 Query: 74 MLFAGRVVDKIGTKTAYVVAICIWSTGAVMHAFAVPMGEGIGAVSSALGIAMIPVSIAGF 133 L G+V+DKIG + + +A IW + HA A + GF Sbjct: 78 YLVWGKVMDKIGARWGFGIAFLIWQVAHIAHAGAR--------------------GLTGF 117 Query: 134 MVSRAVLAIGEAGNFPIAIKATAEYFPKKERSFATGIFNSGANVGAILAPICVPLIASLW 193 + +R L +GEAG FP IKA E+FPKKER+FATGIFN+G N+GAI+ P+ VP I W Sbjct: 118 IFARMALGVGEAGGFPGGIKAVTEWFPKKERAFATGIFNAGTNIGAIVTPLVVPAIVLAW 177 Query: 194 GWEAAFIVIGMLGFVWVGVWIALYEKPEQQKRLSAQELAYIRSDQVVPVVTRPVPGVADK 253 GW+ AFIV G+ G +W+ +W+ +Y P + K LSA ELA+I D PV + Sbjct: 178 GWQMAFIVTGVAGLIWLPIWLLVYRTPRETKNLSAAELAHIEQDPADPV----------E 227 Query: 254 KVSWFKLLTYRQTWAFAFGKFMTDGVWWFFLFWLPTYLSAQYGMKGQAIVMPLAVLYSMT 313 K++W KLLT R+TWA+A GKF+ D +WW FLFWLP +L +YG+ + P+ +Y ++ Sbjct: 228 KIAWTKLLTKRETWAYAIGKFLIDPIWWMFLFWLPDFLGKRYGLDLKTFGPPIVAIYLLS 287 Query: 314 MIGSIGGGWFPSYFMSRGDAPYDGRMKAMLVIAFFPLLVLLAQPLGYISF----WVPVLL 369 GS+GGGW S FM G + R ML+ A LLA P+ + SF WV VL+ Sbjct: 288 DAGSVGGGWLSSNFMKMGWSINRARKITMLICA------LLAVPVMFASFADSLWVAVLI 341 Query: 370 IGVGASAHQAWSCNIFTTVSDMFPQKSIASVVGIGGLAGGLGGVVMTKIGGWVIDHYKLI 429 IGV +AHQ +S N++T SD+FP+ ++ SVVGIGG+ G +GG+V +K G V++ I Sbjct: 342 IGVATAAHQGFSANLYTLPSDVFPRGAVGSVVGIGGMLGAVGGMVFSKYIGGVLES---I 398 Query: 430 GDIHTGYMIMFAICALAYLVAWSVMKALVPRHKEI 464 G Y +F + AYL+A V+ L P+ + + Sbjct: 399 GT----YTPIFIVAGSAYLLALLVVHLLTPKMEPV 429 Lambda K H 0.327 0.140 0.449 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: 721 Number of extensions: 32 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: 467 Length of database: 431 Length adjustment: 33 Effective length of query: 434 Effective length of database: 398 Effective search space: 172732 Effective search space used: 172732 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: 51 (24.3 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.
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:
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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