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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 6 |
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005802 | trans-Golgi network | 4 | 1 |
GO:0031984 | organelle subcompartment | 2 | 1 |
GO:0098791 | Golgi apparatus subcompartment | 3 | 1 |
Related structures:
AlphaFold database: A0A3S7X055
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 7 |
GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016192 | vesicle-mediated transport | 4 | 7 |
GO:0046907 | intracellular transport | 3 | 7 |
GO:0048193 | Golgi vesicle transport | 5 | 7 |
GO:0051179 | localization | 1 | 7 |
GO:0051234 | establishment of localization | 2 | 7 |
GO:0051641 | cellular localization | 2 | 7 |
GO:0051649 | establishment of localization in cell | 3 | 7 |
GO:0006906 | vesicle fusion | 6 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007030 | Golgi organization | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016050 | vesicle organization | 5 | 1 |
GO:0048280 | vesicle fusion with Golgi apparatus | 6 | 1 |
GO:0048284 | organelle fusion | 5 | 1 |
GO:0061024 | membrane organization | 4 | 1 |
GO:0061025 | membrane fusion | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090174 | organelle membrane fusion | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.548 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.475 |
DEG_SPOP_SBC_1 | 103 | 107 | PF00917 | 0.748 |
DEG_SPOP_SBC_1 | 123 | 127 | PF00917 | 0.703 |
DOC_CDC14_PxL_1 | 513 | 521 | PF14671 | 0.312 |
DOC_CYCLIN_RxL_1 | 432 | 439 | PF00134 | 0.312 |
DOC_CYCLIN_yCln2_LP_2 | 220 | 226 | PF00134 | 0.664 |
DOC_CYCLIN_yCln2_LP_2 | 398 | 404 | PF00134 | 0.312 |
DOC_MAPK_MEF2A_6 | 444 | 451 | PF00069 | 0.607 |
DOC_MAPK_MEF2A_6 | 480 | 489 | PF00069 | 0.278 |
DOC_MAPK_NFAT4_5 | 480 | 488 | PF00069 | 0.275 |
DOC_PIKK_1 | 359 | 367 | PF02985 | 0.613 |
DOC_PP1_RVXF_1 | 415 | 421 | PF00149 | 0.367 |
DOC_PP4_FxxP_1 | 354 | 357 | PF00568 | 0.607 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.255 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.705 |
DOC_USP7_MATH_2 | 16 | 22 | PF00917 | 0.692 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.667 |
LIG_14-3-3_CanoR_1 | 56 | 60 | PF00244 | 0.698 |
LIG_Actin_WH2_2 | 465 | 482 | PF00022 | 0.534 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.701 |
LIG_CtBP_PxDLS_1 | 279 | 283 | PF00389 | 0.678 |
LIG_EH_1 | 382 | 386 | PF12763 | 0.607 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.341 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.466 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.686 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.340 |
LIG_GBD_Chelix_1 | 452 | 460 | PF00786 | 0.444 |
LIG_LIR_Apic_2 | 11 | 16 | PF02991 | 0.686 |
LIG_LIR_Apic_2 | 118 | 123 | PF02991 | 0.706 |
LIG_LIR_Gen_1 | 509 | 520 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 523 | 531 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 421 | 427 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 455 | 461 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 509 | 515 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 523 | 528 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 82 | 86 | PF02991 | 0.703 |
LIG_LYPXL_S_1 | 515 | 519 | PF13949 | 0.312 |
LIG_LYPXL_yS_3 | 516 | 519 | PF13949 | 0.312 |
LIG_MYND_3 | 361 | 365 | PF01753 | 0.608 |
LIG_NRBOX | 407 | 413 | PF00104 | 0.312 |
LIG_Pex14_2 | 521 | 525 | PF04695 | 0.312 |
LIG_PTB_Apo_2 | 106 | 113 | PF02174 | 0.749 |
LIG_PTB_Phospho_1 | 106 | 112 | PF10480 | 0.750 |
LIG_REV1ctd_RIR_1 | 431 | 439 | PF16727 | 0.312 |
LIG_SH2_CRK | 13 | 17 | PF00017 | 0.688 |
LIG_SH2_CRK | 458 | 462 | PF00017 | 0.312 |
LIG_SH2_PTP2 | 120 | 123 | PF00017 | 0.707 |
LIG_SH2_SRC | 13 | 16 | PF00017 | 0.707 |
LIG_SH2_STAP1 | 291 | 295 | PF00017 | 0.708 |
LIG_SH2_STAT3 | 236 | 239 | PF00017 | 0.716 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.707 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.772 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.702 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.683 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.681 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.693 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.706 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.591 |
LIG_SH3_3 | 511 | 517 | PF00018 | 0.312 |
LIG_SUMO_SIM_anti_2 | 407 | 413 | PF11976 | 0.352 |
LIG_TRFH_1 | 458 | 462 | PF08558 | 0.312 |
LIG_TYR_ITIM | 456 | 461 | PF00017 | 0.312 |
LIG_TYR_ITIM | 514 | 519 | PF00017 | 0.312 |
LIG_UBA3_1 | 411 | 417 | PF00899 | 0.316 |
LIG_WRC_WIRS_1 | 522 | 527 | PF05994 | 0.340 |
LIG_WW_3 | 175 | 179 | PF00397 | 0.702 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.695 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.698 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.752 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.731 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.769 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.670 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.724 |
MOD_CMANNOS | 492 | 495 | PF00535 | 0.312 |
MOD_Cter_Amidation | 168 | 171 | PF01082 | 0.456 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.501 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.526 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.636 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.543 |
MOD_GlcNHglycan | 190 | 194 | PF01048 | 0.551 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.601 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.444 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.529 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.516 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.535 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.595 |
MOD_GlcNHglycan | 292 | 296 | PF01048 | 0.494 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.437 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.496 |
MOD_GlcNHglycan | 326 | 330 | PF01048 | 0.503 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.519 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.490 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.475 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.468 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.444 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.483 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.705 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.668 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.708 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.726 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.677 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.782 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.768 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.737 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.673 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.723 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.255 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.773 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.703 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.680 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.688 |
MOD_N-GLC_1 | 123 | 128 | PF02516 | 0.534 |
MOD_N-GLC_1 | 146 | 151 | PF02516 | 0.501 |
MOD_N-GLC_1 | 197 | 202 | PF02516 | 0.530 |
MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.520 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.729 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.673 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.312 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.331 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.262 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.388 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.712 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.702 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.706 |
MOD_PK_1 | 386 | 392 | PF00069 | 0.629 |
MOD_PKA_1 | 170 | 176 | PF00069 | 0.650 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.757 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.710 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.759 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.745 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.667 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.679 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.791 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.743 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.312 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.303 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.340 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.312 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.312 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.725 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.755 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.616 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.668 |
TRG_DiLeu_BaEn_1 | 509 | 514 | PF01217 | 0.492 |
TRG_DiLeu_BaLyEn_6 | 313 | 318 | PF01217 | 0.572 |
TRG_DiLeu_BaLyEn_6 | 359 | 364 | PF01217 | 0.614 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 516 | 519 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 522 | 525 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.706 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 55 | 57 | PF00400 | 0.739 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.761 |
TRG_Pf-PMV_PEXEL_1 | 316 | 320 | PF00026 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 347 | 351 | PF00026 | 0.416 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAG4 | Leptomonas seymouri | 48% | 95% |
A4HF64 | Leishmania braziliensis | 78% | 100% |
A4I2E7 | Leishmania infantum | 100% | 100% |
E9AYK0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q8X2 | Leishmania major | 94% | 100% |