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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I3P9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006869 | lipid transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0008289 | lipid binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 397 | 401 | PF00656 | 0.691 |
CLV_MEL_PAP_1 | 323 | 329 | PF00089 | 0.516 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.447 |
DEG_APCC_DBOX_1 | 325 | 333 | PF00400 | 0.531 |
DEG_SCF_FBW7_1 | 80 | 87 | PF00400 | 0.556 |
DEG_SPOP_SBC_1 | 267 | 271 | PF00917 | 0.636 |
DOC_CKS1_1 | 81 | 86 | PF01111 | 0.570 |
DOC_MAPK_MEF2A_6 | 114 | 123 | PF00069 | 0.536 |
DOC_MAPK_MEF2A_6 | 319 | 327 | PF00069 | 0.489 |
DOC_PP1_RVXF_1 | 123 | 129 | PF00149 | 0.521 |
DOC_PP2B_LxvP_1 | 433 | 436 | PF13499 | 0.485 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.536 |
DOC_SPAK_OSR1_1 | 297 | 301 | PF12202 | 0.428 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.724 |
DOC_USP7_MATH_2 | 62 | 68 | PF00917 | 0.686 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.618 |
LIG_14-3-3_CanoR_1 | 297 | 303 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 326 | 330 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 440 | 446 | PF00244 | 0.558 |
LIG_Actin_WH2_2 | 311 | 328 | PF00022 | 0.513 |
LIG_Actin_WH2_2 | 414 | 432 | PF00022 | 0.506 |
LIG_BRCT_BRCA1_1 | 220 | 224 | PF00533 | 0.572 |
LIG_BRCT_BRCA1_1 | 385 | 389 | PF00533 | 0.615 |
LIG_BRCT_BRCA1_1 | 64 | 68 | PF00533 | 0.690 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.671 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.532 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.441 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.574 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.771 |
LIG_LIR_Apic_2 | 354 | 359 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 131 | 140 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 341 | 348 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 387 | 398 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 341 | 346 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.578 |
LIG_PCNA_yPIPBox_3 | 337 | 349 | PF02747 | 0.447 |
LIG_Pex14_2 | 389 | 393 | PF04695 | 0.591 |
LIG_PTB_Apo_2 | 35 | 42 | PF02174 | 0.567 |
LIG_PTB_Phospho_1 | 35 | 41 | PF10480 | 0.565 |
LIG_SH2_CRK | 81 | 85 | PF00017 | 0.572 |
LIG_SH2_GRB2like | 411 | 414 | PF00017 | 0.574 |
LIG_SH2_PTP2 | 343 | 346 | PF00017 | 0.383 |
LIG_SH2_SRC | 120 | 123 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.684 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.574 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.669 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.534 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.471 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.496 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.464 |
LIG_TYR_ITIM | 118 | 123 | PF00017 | 0.542 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.685 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.637 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.597 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.591 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.684 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.607 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.537 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.628 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.637 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.648 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.681 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.665 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.588 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.749 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.679 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.709 |
MOD_GlcNHglycan | 405 | 410 | PF01048 | 0.730 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.634 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.828 |
MOD_GlcNHglycan | 71 | 75 | PF01048 | 0.585 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.611 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.747 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.537 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.619 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.650 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.639 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.642 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.761 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.726 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.535 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.531 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.741 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.692 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.576 |
MOD_N-GLC_1 | 215 | 220 | PF02516 | 0.581 |
MOD_N-GLC_2 | 351 | 353 | PF02516 | 0.388 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.694 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.374 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.406 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.503 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.600 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.558 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.619 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.488 |
MOD_NEK2_2 | 259 | 264 | PF00069 | 0.586 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.741 |
MOD_PIKK_1 | 415 | 421 | PF00454 | 0.434 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.744 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.509 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.467 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.509 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.586 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.514 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.718 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.539 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.447 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.452 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.626 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.707 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.511 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.635 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.649 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.586 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.515 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.616 |
TRG_DiLeu_BaEn_2 | 415 | 421 | PF01217 | 0.514 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.588 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P822 | Leptomonas seymouri | 56% | 72% |
A0A3S7X1N8 | Leishmania donovani | 99% | 72% |
A4HGM5 | Leishmania braziliensis | 69% | 100% |
D0A8B3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AZZ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q894 | Leishmania major | 92% | 99% |