Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 3, no: 7 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0000139 | Golgi membrane | 5 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0098588 | bounding membrane of organelle | 4 | 2 |
Related structures:
AlphaFold database: A4ICR7
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 5 |
GO:0009987 | cellular process | 1 | 4 |
GO:0051179 | localization | 1 | 5 |
GO:0051234 | establishment of localization | 2 | 5 |
GO:0055085 | transmembrane transport | 2 | 4 |
GO:0008643 | carbohydrate transport | 5 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 4 |
GO:0022857 | transmembrane transporter activity | 2 | 4 |
GO:0005338 | nucleotide-sugar transmembrane transporter activity | 4 | 2 |
GO:0015165 | pyrimidine nucleotide-sugar transmembrane transporter activity | 5 | 2 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 2 |
GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 32 | 36 | PF00656 | 0.274 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.420 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.283 |
DOC_CDC14_PxL_1 | 243 | 251 | PF14671 | 0.475 |
DOC_MAPK_DCC_7 | 242 | 251 | PF00069 | 0.461 |
DOC_MAPK_gen_1 | 433 | 442 | PF00069 | 0.552 |
DOC_MAPK_MEF2A_6 | 242 | 251 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 332 | 339 | PF00069 | 0.384 |
DOC_PP1_RVXF_1 | 199 | 206 | PF00149 | 0.346 |
DOC_PP2B_LxvP_1 | 311 | 314 | PF13499 | 0.352 |
DOC_PP2B_LxvP_1 | 377 | 380 | PF13499 | 0.326 |
DOC_PP4_FxxP_1 | 40 | 43 | PF00568 | 0.410 |
DOC_PP4_FxxP_1 | 61 | 64 | PF00568 | 0.243 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.304 |
LIG_14-3-3_CanoR_1 | 100 | 107 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 368 | 373 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 56 | 62 | PF00244 | 0.359 |
LIG_Actin_WH2_2 | 16 | 31 | PF00022 | 0.363 |
LIG_BIR_III_2 | 423 | 427 | PF00653 | 0.498 |
LIG_BRCT_BRCA1_1 | 340 | 344 | PF00533 | 0.320 |
LIG_BRCT_BRCA1_1 | 36 | 40 | PF00533 | 0.355 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.303 |
LIG_EH1_1 | 386 | 394 | PF00400 | 0.165 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.349 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.469 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.467 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.236 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.359 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.521 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.637 |
LIG_FHA_2 | 447 | 453 | PF00498 | 0.613 |
LIG_LIR_Apic_2 | 115 | 120 | PF02991 | 0.515 |
LIG_LIR_Apic_2 | 124 | 129 | PF02991 | 0.270 |
LIG_LIR_Apic_2 | 37 | 43 | PF02991 | 0.392 |
LIG_LIR_Apic_2 | 60 | 64 | PF02991 | 0.262 |
LIG_LIR_Gen_1 | 145 | 155 | PF02991 | 0.262 |
LIG_LIR_Gen_1 | 159 | 169 | PF02991 | 0.238 |
LIG_LIR_Gen_1 | 384 | 395 | PF02991 | 0.226 |
LIG_LIR_Gen_1 | 411 | 421 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 7 | 18 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 411 | 416 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 7 | 13 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.340 |
LIG_MLH1_MIPbox_1 | 340 | 344 | PF16413 | 0.320 |
LIG_NRBOX | 194 | 200 | PF00104 | 0.303 |
LIG_NRBOX | 217 | 223 | PF00104 | 0.379 |
LIG_NRBOX | 335 | 341 | PF00104 | 0.245 |
LIG_NRBOX | 373 | 379 | PF00104 | 0.464 |
LIG_PCNA_yPIPBox_3 | 212 | 222 | PF02747 | 0.251 |
LIG_Pex14_2 | 383 | 387 | PF04695 | 0.283 |
LIG_Pex14_2 | 61 | 65 | PF04695 | 0.256 |
LIG_PTB_Apo_2 | 399 | 406 | PF02174 | 0.379 |
LIG_SH2_CRK | 117 | 121 | PF00017 | 0.549 |
LIG_SH2_CRK | 148 | 152 | PF00017 | 0.259 |
LIG_SH2_CRK | 232 | 236 | PF00017 | 0.257 |
LIG_SH2_CRK | 244 | 248 | PF00017 | 0.435 |
LIG_SH2_NCK_1 | 148 | 152 | PF00017 | 0.271 |
LIG_SH2_PTP2 | 91 | 94 | PF00017 | 0.477 |
LIG_SH2_SRC | 315 | 318 | PF00017 | 0.305 |
LIG_SH2_STAP1 | 148 | 152 | PF00017 | 0.271 |
LIG_SH2_STAP1 | 315 | 319 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.499 |
LIG_SH3_1 | 117 | 123 | PF00018 | 0.527 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.533 |
LIG_SUMO_SIM_anti_2 | 263 | 268 | PF11976 | 0.326 |
LIG_SUMO_SIM_par_1 | 359 | 366 | PF11976 | 0.546 |
LIG_TRAF2_1 | 284 | 287 | PF00917 | 0.303 |
LIG_TRAF2_2 | 418 | 423 | PF00917 | 0.494 |
LIG_TYR_ITIM | 146 | 151 | PF00017 | 0.269 |
LIG_TYR_ITIM | 313 | 318 | PF00017 | 0.305 |
LIG_UBA3_1 | 240 | 245 | PF00899 | 0.471 |
LIG_WRC_WIRS_1 | 58 | 63 | PF05994 | 0.278 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.494 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.328 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.721 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.364 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.387 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.607 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.372 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.191 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.704 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.379 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.335 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.486 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.395 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.617 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.553 |
MOD_N-GLC_1 | 368 | 373 | PF02516 | 0.338 |
MOD_N-GLC_2 | 346 | 348 | PF02516 | 0.291 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.226 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.368 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.266 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.283 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.467 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.379 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.306 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.337 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.312 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.451 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.467 |
MOD_OFUCOSY | 73 | 78 | PF10250 | 0.245 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.335 |
MOD_PKA_1 | 100 | 106 | PF00069 | 0.590 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.479 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.367 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.680 |
MOD_PKB_1 | 445 | 453 | PF00069 | 0.592 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.358 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.384 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.624 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.245 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.458 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.229 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.270 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.247 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.330 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.374 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.378 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.441 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.285 |
MOD_Plk_4 | 378 | 384 | PF00069 | 0.345 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.321 |
MOD_SUMO_for_1 | 440 | 443 | PF00179 | 0.578 |
MOD_SUMO_rev_2 | 327 | 334 | PF00179 | 0.227 |
TRG_DiLeu_BaEn_1 | 75 | 80 | PF01217 | 0.326 |
TRG_DiLeu_BaEn_2 | 329 | 335 | PF01217 | 0.270 |
TRG_DiLeu_BaLyEn_6 | 236 | 241 | PF01217 | 0.506 |
TRG_DiLeu_BaLyEn_6 | 53 | 58 | PF01217 | 0.279 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.323 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAC3 | Leptomonas seymouri | 59% | 99% |
A0A0S4JLV3 | Bodo saltans | 32% | 100% |
A0A0S4JVX5 | Bodo saltans | 32% | 100% |
A0A1X0P938 | Trypanosomatidae | 48% | 100% |
A0A3Q8INC1 | Leishmania donovani | 100% | 100% |
A0A3R7N2L5 | Trypanosoma rangeli | 48% | 100% |
A4HNS7 | Leishmania braziliensis | 74% | 100% |
E9ASI7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q209 | Leishmania major | 93% | 100% |
Q5RFT1 | Pongo abelii | 30% | 100% |
Q5RKH7 | Rattus norvegicus | 30% | 100% |
Q8N357 | Homo sapiens | 30% | 100% |
Q8VE96 | Mus musculus | 29% | 100% |