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:0000139 | Golgi membrane | 5 | 2 |
GO:0016020 | membrane | 2 | 6 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0031984 | organelle subcompartment | 2 | 2 |
GO:0031985 | Golgi cisterna | 4 | 2 |
GO:0098588 | bounding membrane of organelle | 4 | 2 |
GO:0098791 | Golgi apparatus subcompartment | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005794 | Golgi apparatus | 5 | 5 |
GO:0043226 | organelle | 2 | 5 |
GO:0043227 | membrane-bounded organelle | 3 | 5 |
GO:0043229 | intracellular organelle | 3 | 5 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 5 |
Related structures:
AlphaFold database: Q4QC83
Term | Name | Level | Count |
---|---|---|---|
GO:0000301 | retrograde transport, vesicle recycling within Golgi | 7 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006891 | intra-Golgi vesicle-mediated transport | 6 | 2 |
GO:0006996 | organelle organization | 4 | 7 |
GO:0007030 | Golgi organization | 5 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016043 | cellular component organization | 3 | 7 |
GO:0016192 | vesicle-mediated transport | 4 | 2 |
GO:0048193 | Golgi vesicle transport | 5 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 169 | 173 | PF00656 | 0.683 |
CLV_C14_Caspase3-7 | 533 | 537 | PF00656 | 0.695 |
CLV_C14_Caspase3-7 | 563 | 567 | PF00656 | 0.591 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.467 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.453 |
CLV_PCSK_PC7_1 | 372 | 378 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 574 | 578 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 584 | 588 | PF00082 | 0.269 |
CLV_Separin_Metazoa | 384 | 388 | PF03568 | 0.621 |
DEG_APCC_DBOX_1 | 371 | 379 | PF00400 | 0.629 |
DEG_APCC_DBOX_1 | 423 | 431 | PF00400 | 0.577 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.670 |
DEG_SPOP_SBC_1 | 490 | 494 | PF00917 | 0.644 |
DEG_SPOP_SBC_1 | 83 | 87 | PF00917 | 0.697 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 430 | 439 | PF00134 | 0.588 |
DOC_MAPK_gen_1 | 339 | 347 | PF00069 | 0.636 |
DOC_MAPK_gen_1 | 422 | 430 | PF00069 | 0.584 |
DOC_MAPK_gen_1 | 538 | 547 | PF00069 | 0.637 |
DOC_MAPK_MEF2A_6 | 341 | 349 | PF00069 | 0.601 |
DOC_MIT_MIM_1 | 300 | 308 | PF04212 | 0.632 |
DOC_PP2B_LxvP_1 | 119 | 122 | PF13499 | 0.671 |
DOC_PP4_FxxP_1 | 487 | 490 | PF00568 | 0.779 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.817 |
DOC_USP7_MATH_1 | 560 | 564 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.761 |
DOC_USP7_UBL2_3 | 202 | 206 | PF12436 | 0.517 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.749 |
LIG_14-3-3_CanoR_1 | 129 | 137 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 223 | 233 | PF00244 | 0.718 |
LIG_14-3-3_CanoR_1 | 282 | 288 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 35 | 42 | PF00244 | 0.702 |
LIG_14-3-3_CanoR_1 | 376 | 386 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 44 | 49 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 574 | 583 | PF00244 | 0.694 |
LIG_AP2alpha_2 | 159 | 161 | PF02296 | 0.644 |
LIG_APCC_ABBA_1 | 254 | 259 | PF00400 | 0.620 |
LIG_BRCT_BRCA1_1 | 483 | 487 | PF00533 | 0.725 |
LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.638 |
LIG_BRCT_BRCA1_1 | 86 | 90 | PF00533 | 0.703 |
LIG_CaM_IQ_9 | 333 | 348 | PF13499 | 0.581 |
LIG_EVH1_1 | 487 | 491 | PF00568 | 0.730 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.649 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.714 |
LIG_FHA_1 | 603 | 609 | PF00498 | 0.369 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.722 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.607 |
LIG_FHA_2 | 527 | 533 | PF00498 | 0.696 |
LIG_GBD_Chelix_1 | 598 | 606 | PF00786 | 0.325 |
LIG_LIR_Apic_2 | 484 | 490 | PF02991 | 0.727 |
LIG_MYND_1 | 54 | 58 | PF01753 | 0.702 |
LIG_PDZ_Class_3 | 619 | 624 | PF00595 | 0.435 |
LIG_SH2_GRB2like | 477 | 480 | PF00017 | 0.600 |
LIG_SH2_PTP2 | 590 | 593 | PF00017 | 0.304 |
LIG_SH2_SRC | 477 | 480 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.304 |
LIG_SH3_2 | 55 | 60 | PF14604 | 0.712 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.631 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.756 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.707 |
LIG_SH3_3 | 617 | 623 | PF00018 | 0.450 |
LIG_SUMO_SIM_par_1 | 117 | 123 | PF11976 | 0.716 |
LIG_SUMO_SIM_par_1 | 557 | 564 | PF11976 | 0.572 |
LIG_SUMO_SIM_par_1 | 604 | 611 | PF11976 | 0.504 |
LIG_TRAF2_2 | 288 | 293 | PF00917 | 0.695 |
LIG_WRC_WIRS_1 | 125 | 130 | PF05994 | 0.615 |
LIG_WRC_WIRS_1 | 565 | 570 | PF05994 | 0.483 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.662 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.594 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.587 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.641 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.479 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.601 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.612 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.604 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.585 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.722 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.433 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.593 |
MOD_GlcNHglycan | 364 | 368 | PF01048 | 0.480 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.501 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.632 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.612 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.584 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.593 |
MOD_GlcNHglycan | 532 | 536 | PF01048 | 0.729 |
MOD_GlcNHglycan | 609 | 613 | PF01048 | 0.504 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.626 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.618 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.613 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.564 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.455 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.646 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.451 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.588 |
MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.486 |
MOD_N-GLC_1 | 44 | 49 | PF02516 | 0.564 |
MOD_N-GLC_2 | 481 | 483 | PF02516 | 0.533 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.670 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.628 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.554 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.594 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.554 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.430 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.598 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.493 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.604 |
MOD_NEK2_2 | 482 | 487 | PF00069 | 0.592 |
MOD_PIKK_1 | 129 | 135 | PF00454 | 0.744 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.704 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.518 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.498 |
MOD_PIKK_1 | 574 | 580 | PF00454 | 0.459 |
MOD_PKA_1 | 387 | 393 | PF00069 | 0.582 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.622 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.553 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.590 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.532 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.558 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.705 |
MOD_PKA_2 | 471 | 477 | PF00069 | 0.601 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.499 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.640 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.565 |
MOD_Plk_2-3 | 13 | 19 | PF00069 | 0.487 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.434 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.613 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.541 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.566 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.571 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.639 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.697 |
MOD_SUMO_rev_2 | 10 | 16 | PF00179 | 0.477 |
MOD_SUMO_rev_2 | 266 | 275 | PF00179 | 0.497 |
MOD_SUMO_rev_2 | 445 | 451 | PF00179 | 0.473 |
TRG_DiLeu_BaLyEn_6 | 260 | 265 | PF01217 | 0.451 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 590 | 593 | PF00928 | 0.304 |
TRG_ER_diArg_1 | 375 | 377 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 386 | 388 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 538 | 540 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 76 | 79 | PF00400 | 0.647 |
TRG_Pf-PMV_PEXEL_1 | 263 | 267 | PF00026 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 299 | 303 | PF00026 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 376 | 381 | PF00026 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 416 | 420 | PF00026 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 574 | 578 | PF00026 | 0.465 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCL5 | Leptomonas seymouri | 40% | 93% |
A0A3Q8IB66 | Leishmania donovani | 91% | 99% |
A4HBX1 | Leishmania braziliensis | 72% | 100% |
A4HZ89 | Leishmania infantum | 91% | 99% |
E9AV97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |