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:0005794 | Golgi apparatus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QGA6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 57 | 63 | PF00089 | 0.609 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.665 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 301 | 303 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.467 |
CLV_Separin_Metazoa | 445 | 449 | PF03568 | 0.518 |
DEG_APCC_DBOX_1 | 215 | 223 | PF00400 | 0.635 |
DEG_SPOP_SBC_1 | 507 | 511 | PF00917 | 0.525 |
DOC_CDC14_PxL_1 | 413 | 421 | PF14671 | 0.691 |
DOC_MAPK_gen_1 | 354 | 360 | PF00069 | 0.690 |
DOC_MAPK_RevD_3 | 398 | 412 | PF00069 | 0.541 |
DOC_PP4_FxxP_1 | 395 | 398 | PF00568 | 0.665 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.713 |
DOC_USP7_UBL2_3 | 96 | 100 | PF12436 | 0.506 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.691 |
LIG_14-3-3_CanoR_1 | 216 | 220 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 250 | 256 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 274 | 280 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 314 | 318 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 448 | 456 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 52 | 58 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 60 | 68 | PF00244 | 0.593 |
LIG_Actin_WH2_2 | 171 | 189 | PF00022 | 0.627 |
LIG_Actin_WH2_2 | 201 | 218 | PF00022 | 0.638 |
LIG_Actin_WH2_2 | 353 | 370 | PF00022 | 0.676 |
LIG_APCC_Cbox_2 | 334 | 340 | PF00515 | 0.646 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.474 |
LIG_EH_1 | 419 | 423 | PF12763 | 0.781 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.553 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.651 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.615 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.698 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.546 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.579 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.638 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.600 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.561 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.676 |
LIG_GBD_Chelix_1 | 161 | 169 | PF00786 | 0.628 |
LIG_LIR_Apic_2 | 394 | 398 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 26 | 34 | PF02991 | 0.618 |
LIG_LIR_Gen_1 | 289 | 298 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 333 | 343 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 26 | 30 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 289 | 293 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 295 | 300 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 333 | 339 | PF02991 | 0.642 |
LIG_MYND_1 | 417 | 421 | PF01753 | 0.689 |
LIG_Pex14_1 | 332 | 336 | PF04695 | 0.638 |
LIG_Pex14_1 | 466 | 470 | PF04695 | 0.552 |
LIG_SH2_CRK | 290 | 294 | PF00017 | 0.602 |
LIG_SH2_CRK | 297 | 301 | PF00017 | 0.538 |
LIG_SH2_CRK | 470 | 474 | PF00017 | 0.560 |
LIG_SH2_STAP1 | 190 | 194 | PF00017 | 0.616 |
LIG_SH2_STAP1 | 290 | 294 | PF00017 | 0.629 |
LIG_SH2_STAT3 | 190 | 193 | PF00017 | 0.631 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.649 |
LIG_SH3_1 | 412 | 418 | PF00018 | 0.537 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.661 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.591 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.664 |
LIG_TRAF2_1 | 125 | 128 | PF00917 | 0.562 |
LIG_TRAF2_1 | 132 | 135 | PF00917 | 0.539 |
LIG_TRAF2_1 | 338 | 341 | PF00917 | 0.641 |
LIG_TRAF2_1 | 63 | 66 | PF00917 | 0.653 |
LIG_UBA3_1 | 88 | 96 | PF00899 | 0.658 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.640 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.635 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.408 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.552 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.721 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.777 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.575 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.533 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.579 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.621 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.544 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.618 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.788 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.633 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.688 |
MOD_Cter_Amidation | 409 | 412 | PF01082 | 0.556 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.644 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.631 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.576 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.639 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.556 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.675 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.747 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.627 |
MOD_GlcNHglycan | 488 | 494 | PF01048 | 0.514 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.549 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.704 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.640 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.566 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.629 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.440 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.595 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.639 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.634 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.616 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.300 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.663 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.647 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.769 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.706 |
MOD_N-GLC_1 | 163 | 168 | PF02516 | 0.394 |
MOD_N-GLC_1 | 220 | 225 | PF02516 | 0.637 |
MOD_N-GLC_1 | 53 | 58 | PF02516 | 0.688 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.552 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.637 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.536 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.634 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.570 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.627 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.704 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.662 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.626 |
MOD_PIKK_1 | 269 | 275 | PF00454 | 0.632 |
MOD_PIKK_1 | 343 | 349 | PF00454 | 0.594 |
MOD_PIKK_1 | 375 | 381 | PF00454 | 0.777 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.636 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.551 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.650 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.646 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.630 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.630 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.505 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.613 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.538 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.712 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.520 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.650 |
MOD_Plk_2-3 | 264 | 270 | PF00069 | 0.560 |
MOD_Plk_2-3 | 289 | 295 | PF00069 | 0.552 |
MOD_Plk_2-3 | 313 | 319 | PF00069 | 0.546 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.552 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.688 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.599 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.591 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.664 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.692 |
MOD_SUMO_rev_2 | 431 | 438 | PF00179 | 0.723 |
TRG_DiLeu_BaEn_1 | 289 | 294 | PF01217 | 0.628 |
TRG_DiLeu_BaEn_1 | 475 | 480 | PF01217 | 0.617 |
TRG_DiLeu_BaEn_4 | 104 | 110 | PF01217 | 0.582 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.629 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.649 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.569 |
TRG_ENDOCYTIC_2 | 484 | 487 | PF00928 | 0.427 |
TRG_ER_diArg_1 | 123 | 126 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 411 | 413 | PF00400 | 0.621 |
TRG_Pf-PMV_PEXEL_1 | 335 | 340 | PF00026 | 0.647 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3R7L520 | Trypanosoma rangeli | 27% | 76% |
A0A3S7WSC1 | Leishmania donovani | 94% | 69% |
A4H737 | Leishmania braziliensis | 78% | 69% |
A4HVH7 | Leishmania infantum | 94% | 100% |
D0A6T4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 81% |
E9AP72 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 74% |